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Tray, Anesthesia, Epidural, Continuous

by Travenol Laboratories, S.A.

510(k) K770571

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 NumberK770571 Date30 Mar 1977ClearedStatusActive

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  • Withdrawn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
CAZ
Device Class
Class II
Regulation
21 CFR Part 868.5140
Advisory Committee
Anesthesiology
FDA Decision
SESE Substantially Equivalent

Overview

AI-generated summary, 27 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 Tray, Anesthesia, Epidural, Continuous is an anesthesia conduction kit used to facilitate the administration of continuous epidural anesthesia. It contains the necessary components to support clinical procedures requiring regional anesthesia.

This device is manufactured by Travenol Laboratories, S.A. and has received FDA 510(k) clearance under the regulation number 868.5140. It is classified as a Class II medical device within the anesthesiology specialty.

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Questions

AI-generated answers, 27 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 this anesthesia tray?

    The Tray, Anesthesia, Epidural, Continuous is designed to facilitate the administration of continuous epidural anesthesia. It serves as a conduction kit containing the necessary components to support clinical procedures that require regional anesthesia.

  • What is the regulatory classification of this device?

    This device is classified as a Class II medical device within the anesthesiology specialty. It has received FDA 510(k) clearance under regulation number 868.5140.

  • Who is the manufacturer of this epidural tray?

    This device is manufactured by Travenol Laboratories, S.A., located in McHenry, Illinois.