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FDA 510(k)

MCBRIDE LISTERIA AGAR W/CYCLOHEXIMIDE, DRI & PRE

K-Number: K870134 · 1987-02-04

ApplicantGibco Laboratories Life Technologies, Inc.
Decision Date1987-02-04
Product CodeJSJ
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

MCBRIDE LISTERIA AGAR W/CYCLOHEXIMIDE, DRI & PRE 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 1987-02-04 under 510(k) number K870134. The device is classified under product code JSJ. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MCBRIDE LISTERIA AGAR W/CYCLOHEXIMIDE, DRI & PRE?

MCBRIDE LISTERIA AGAR W/CYCLOHEXIMIDE, DRI & PRE is a medical device that received FDA 510(k) clearance on 1987-02-04. The listed applicant is Gibco Laboratories Life Technologies, Inc.. The 510(k) number is K870134.

When did MCBRIDE LISTERIA AGAR W/CYCLOHEXIMIDE, DRI & PRE receive FDA 510(k) clearance?

MCBRIDE LISTERIA AGAR W/CYCLOHEXIMIDE, DRI & PRE received FDA 510(k) clearance on 1987-02-04, under 510(k) number K870134.

Who is the listed applicant for MCBRIDE LISTERIA AGAR W/CYCLOHEXIMIDE, DRI & PRE?

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 MCBRIDE LISTERIA AGAR W/CYCLOHEXIMIDE, DRI & PRE?

The FDA product code for MCBRIDE LISTERIA AGAR W/CYCLOHEXIMIDE, DRI & PRE is JSJ.

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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 C0226K864755PSEUDOMONAS CEPACIA SELECTIVE AGAR, DRI & PRE-FORMK864014LOMBARD DOWELL AGAR BASEK863821MUELLER HINTON AGAR W/4%NACL AND OXACILLINK863820DRI-FORM: GBNA LISTERIA MEDIUM NO. M22300

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Related Devices (Code: JSJ)

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.

K882463POTATO DEXTROSE AGAR (PDA) - PRODUCT #P3421Lakewood Biochemical Co., Inc.K881544LITTMAN AGARAcumedia Manufacturers, Inc.K881561TERGITOL 7 BROTHAcumedia Manufacturers, Inc.K881526CHAPMAN STONE MEDIUMAcumedia Manufacturers, Inc.K881571YM BROTHAcumedia Manufacturers, Inc.K881578STREPTOSELAcumedia Manufacturers, 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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