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FDA 510(k)

BCYE MEDIUM

K-Number: K812911 · 1981-11-06

ApplicantGibco Laboratories Life Technologies, Inc.
Decision Date1981-11-06
Product CodeJSE
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

BCYE MEDIUM 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 1981-11-06 under 510(k) number K812911. The device is classified under product code JSE. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BCYE MEDIUM?

BCYE MEDIUM is a medical device that received FDA 510(k) clearance on 1981-11-06. The listed applicant is Gibco Laboratories Life Technologies, Inc.. The 510(k) number is K812911.

When did BCYE MEDIUM receive FDA 510(k) clearance?

BCYE MEDIUM received FDA 510(k) clearance on 1981-11-06, under 510(k) number K812911.

Who is the listed applicant for BCYE MEDIUM?

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 BCYE MEDIUM?

The FDA product code for BCYE MEDIUM is JSE.

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

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K871855SORBITOL MACCONKEY (SMAC) AGAR, DRI & PRE-FORMK871541MARTIN-LEWIS AGAR W/REDUCED VANCOMYCIN C0226K870134MCBRIDE LISTERIA AGAR W/CYCLOHEXIMIDE, DRI & PREK864755PSEUDOMONAS CEPACIA SELECTIVE AGAR, DRI & PRE-FORMK864014LOMBARD DOWELL AGAR BASEK863821MUELLER HINTON AGAR W/4%NACL AND OXACILLIN

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Related Devices (Code: JSE)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K962265MLX MICROTITER PLATE LUMINOMETERDynatech Laboratories, Inc.K883995X-ACT UREA/TDAPro-Lab, Inc.K883996X-ACT LDC/INDPro-Lab, Inc.K880133MIL MEDIUMHardy MediaK880116MRVP BROTHHardy MediaK874537KLIGLER IRON AGAR AND TRIPLE SUGAR IRON AGARLakewood Biochemical Co., Inc.

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.

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