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FDA 510(k)

CHOCOLATE AGAR

K-Number: K864238 · 1987-03-31

ApplicantMds Laboratories, Inc.
Decision Date1987-03-31
Product CodeKZI
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

CHOCOLATE AGAR is the device name listed in this FDA 510(k) record. The listed applicant is Mds Laboratories, Inc.. It received FDA 510(k) clearance on 1987-03-31 under 510(k) number K864238. The device is classified under product code KZI. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHOCOLATE AGAR?

CHOCOLATE AGAR is a medical device that received FDA 510(k) clearance on 1987-03-31. The listed applicant is Mds Laboratories, Inc.. The 510(k) number is K864238.

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

CHOCOLATE AGAR received FDA 510(k) clearance on 1987-03-31, under 510(k) number K864238.

Who is the listed applicant for CHOCOLATE AGAR?

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

What is the FDA product code for CHOCOLATE AGAR?

The FDA product code for CHOCOLATE AGAR is KZI.

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Other records listing Mds Laboratories, 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.

K864241DNASE AGARK864242HEKTOEN ENTERIC AGARK864252THAYER-MARTIN JEMBECK864247MUELLER HINTON AGAR WITH 5% SHEEP BLOODK864244GARNERELLA VAGINALIS IDENTIFICATION KITK864249NORMAL SALINE STERILE

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Related Devices (Code: KZI)

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.

K884208LISTERIA SELECTIVE MEDIUM (OXFORD FORMULATION)Oxoid U.S.A., Inc.K881995DIAMOND'S MEDIUM MODIFIEDRemel Co.K880122MIDDLEBROOK 7H9 BROTHHardy MediaK880131LOWENSTEIN-JENSEN, GRUFTHardy MediaK880134MIDDLEBROOK 7H11 AGARHardy MediaK880138WALLENSTEIN MEDIUM SLANTHardy Media

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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