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FDA 510(k)

CHOCOLATE AGAR

K-Number: K851588 · 1985-04-30

ApplicantPreferred Micro-Media
Decision Date1985-04-30
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 Preferred Micro-Media. It received FDA 510(k) clearance on 1985-04-30 under 510(k) number K851588. 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 1985-04-30. The listed applicant is Preferred Micro-Media. The 510(k) number is K851588.

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

CHOCOLATE AGAR received FDA 510(k) clearance on 1985-04-30, under 510(k) number K851588.

Who is the listed applicant for CHOCOLATE AGAR?

The FDA 510(k) record lists Preferred Micro-Media 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 Preferred Micro-Media 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.

K851594SF BROTHK851595SIMMONS CITRATE AGARK851597TRIPLE SUGAR IRON AGARK851593SELECTIVE STREPTOCOCCUS AGARK851592SABOURAUD DEXTROSE AGARK851596SIM MEDIUM

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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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