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Minrad Nasal Scavenging Circuit

by Minrad, Inc.

510(k) K072255

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 6 Oct 2026

Documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source FDA 510(k), synced 6 Oct 2026. What this means

Regulatory status

as of registry sync 6 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK072255 Date18 Oct 2007ClearedStatusActive

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 6 Oct 2026.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

510(k)

Full name
Minrad Inc. Nasal Scavenging Circuit
510(k) Number
FDA Product Code
CBN
Device Class
Class II
Regulation
21 CFR Part 868.5430
Advisory Committee
Anesthesiology
FDA Decision
SESE Substantially Equivalent

Overview

AI-generated summary, 19 Sep 2026

Written by a language model from registry data. Not verified by deviCERTS or the manufacturer. The registry data above is the record.

The Minrad Nasal Scavenging Circuit is an Apparatus, Gas-Scavenging designed for use in anesthesiology. It is intended to deliver medical gases—such as analgesic agents, oxygen, or air—to patients while simultaneously removing expired gases and excess unused gases from the treatment environment, ensuring a controlled and safe procedural space.

This device is supplied as a single-use nasal scavenging circuit and connects to conscious sedation systems. It is classified as a Class II medical device under FDA regulation 868.5430, with a 510(k) clearance (K072255) for substantial equivalence. No additional sterility or MRI safety information is specified in the available data.

Other devices from Minrad, Inc.

See all devices from Minrad, Inc. →

Questions

AI-generated answers, 19 Sep 2026

Written by a language model from registry data. Not verified by deviCERTS or the manufacturer. The registry data above is the record.

  • What is the primary purpose of the Minrad Nasal Scavenging Circuit in clinical settings?

    The Minrad Nasal Scavenging Circuit is designed specifically for use in anesthesiology to deliver medical gases—such as oxygen, air, or analgesic agents—to patients during procedures. Simultaneously, it removes expired gases and excess unused gases from the patient’s environment, helping maintain a controlled and safe procedural space. This is particularly useful in conscious sedation systems where gas management is critical.

  • Is the Minrad Nasal Scavenging Circuit intended for single-use or repeated use?

    The Minrad Nasal Scavenging Circuit is explicitly supplied as a single-use device. This design ensures patient safety and hygiene, as it is not intended for reuse or reprocessing. Always follow the manufacturer’s instructions for proper disposal after a single use.

  • What types of medical gases can be used with this device, and how is it connected?

    This device is intended for use with common anesthetic gases, including oxygen, air, and analgesic agents. It connects directly to conscious sedation systems and is designed to integrate seamlessly into existing anesthesia workflows. The circuit ensures efficient scavenging of expired gases while delivering fresh gas mixtures to the patient.

  • Are there multiple sizes or models available for the Minrad Nasal Scavenging Circuit?

    Yes, the Minrad Nasal Scavenging Circuit comes in multiple registration numbers and product codes, indicating variations in design or configuration. These include registration numbers like 3008776780, 3007143859, 2243990, and others, which may correspond to different sizes, flow rates, or compatibility with specific sedation systems. Always verify the correct model for your clinical application.

  • How should the Minrad Nasal Scavenging Circuit be stored before use?

    Since the device is single-use and no specific sterility requirements beyond standard single-use medical device handling are mentioned, it should be stored in a clean, dry environment protected from contamination. Follow the manufacturer’s packaging instructions to preserve integrity until use. Avoid exposure to extreme temperatures or direct sunlight.