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Filter, Respiratory (U-MID)

by Bd Becton Dickinson Vacutainer Systems Preanalytic

510(k) K760041

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source FDA 510(k), synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK760041 Date16 Jul 1976ClearedStatusActive

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA Product Code
CAH
Device Class
Class II
Regulation
21 CFR Part 868.5260
Advisory Committee
Anesthesiology
FDA Decision
SESE Substantially Equivalent

Overview

AI-generated summary, 25 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 Filter, Respiratory (U-MID) is a bacterial filter designed for breathing circuits. It is classified as a Filter, Bacterial, Breathing-Circuit under product code CAH and is intended for use in medical settings.

This device is Class II with special controls and was cleared by the FDA on July 16, 1976, under 510(k) number K760041. It is manufactured by BD Becton Dickinson Vacutainer Systems Preanalytic and is regulated under 868.5260. The device is intended for use in anesthesiology applications.

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