BRUCELLA BROTH W/SPS, 6% SORBITOL & CO2— 510(k) K790687

Name: FDA 510(k) clearance K790687
Creator: U.S. Food and Drug Administration
Published: 1979-05-03

Substantially Equivalent

Gibco Laboratories Life Technologies, Inc.

FDA 510(k) clearance K790687 for BRUCELLA BROTH W/SPS, 6% SORBITOL & CO2, Substantially Equivalent on 1979-05-03. Applicant: Gibco Laboratories Life Technologies, Inc.. Device class: 1.

Clearance details

Applicant: Gibco Laboratories Life Technologies, Inc.
Product code: Code JSC
Device class: Class 1
Regulation: 21 CFR 866.2350
Advisory panel: Microbiology
Date received: 1979-04-10
Decision date: 1979-05-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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K870134 — MCBRIDE LISTERIA AGAR W/CYCLOHEXIMIDE, DRI & PRE1987-02-04
K864755 — PSEUDOMONAS CEPACIA SELECTIVE AGAR, DRI & PRE-FORM1987-01-05
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Recalls naming K790687

K-number listed on FDA's recall record

Z-0585-2026 — 1. CAMHB W/LHB, MANUAL, 11ML, 10/BOX YCP112-10 2. BRUCELLA BROTH, 11ML, 10/BOX YT3450Class II·Ongoing·Remel, Inc·20251112

Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K790687.

Data sourced from openFDA. This site is unofficial and independent of the FDA.