FDA 510(k)

ACETAMIDE AGAR

K-Number: K830020 · 1983-02-07

ApplicantGibco Laboratories Life Technologies, Inc.

Decision Date1983-02-07

Product CodeJSH

Advisory CommitteeMI

DecisionSubstantially Equivalent

Device Summary

ACETAMIDE AGAR is the device name listed in this FDA 510(k) record. The listed applicant is Gibco Laboratories Life Technologies, Inc.. It received FDA 510(k) clearance on 1983-02-07 under 510(k) number K830020. The device is classified under product code JSH. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACETAMIDE AGAR?

ACETAMIDE AGAR is a medical device that received FDA 510(k) clearance on 1983-02-07. The listed applicant is Gibco Laboratories Life Technologies, Inc.. The 510(k) number is K830020.

When did ACETAMIDE AGAR receive FDA 510(k) clearance?

ACETAMIDE AGAR received FDA 510(k) clearance on 1983-02-07, under 510(k) number K830020.

Who is the listed applicant for ACETAMIDE AGAR?

The FDA 510(k) record lists Gibco Laboratories Life Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ACETAMIDE AGAR?

The FDA product code for ACETAMIDE AGAR is JSH.

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Other records listing Gibco Laboratories Life Technologies, Inc. as applicant

K871855SORBITOL MACCONKEY (SMAC) AGAR, DRI & PRE-FORM K871541MARTIN-LEWIS AGAR W/REDUCED VANCOMYCIN C0226 K870134MCBRIDE LISTERIA AGAR W/CYCLOHEXIMIDE, DRI & PRE K864755PSEUDOMONAS CEPACIA SELECTIVE AGAR, DRI & PRE-FORM K864014LOMBARD DOWELL AGAR BASE K863821MUELLER HINTON AGAR W/4%NACL AND OXACILLIN

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.