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Mueller Hinton Broth

by Gibco Laboratories Life Technologies, Inc. 510(k)

Active United States Open recall

510(k) K802957

Regulatory status

as of 28 Oct 2026

Recall ongoing. 1 ongoing FDA recall names this device. See recalls

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK802957 Date22 Dec 1980ClearedStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Recalls

1 recall · 1 ongoing · FDA

    • Ongoing Z-0585-2026 FDA Class II initiated 12 Nov 2025

    Products may contain contamination, which may result in a darker or brown media color.

Specification

510(k)

510(k) Number
FDA Product Code
JTZ
Device Class
Class II
Regulation
21 CFR Part 866.1700
Advisory Committee
Microbiology
FDA Decision
SESE Substantially Equivalent

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