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FDA 510(k)

SHEEP BLOOD AGAR

K-Number: K841748 · 1984-05-31

ApplicantThe Montana Deaconess Medical Center
Decision Date1984-05-31
Product CodeKZI
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

SHEEP BLOOD AGAR is the device name listed in this FDA 510(k) record. The listed applicant is The Montana Deaconess Medical Center. It received FDA 510(k) clearance on 1984-05-31 under 510(k) number K841748. 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 SHEEP BLOOD AGAR?

SHEEP BLOOD AGAR is a medical device that received FDA 510(k) clearance on 1984-05-31. The listed applicant is The Montana Deaconess Medical Center. The 510(k) number is K841748.

When did SHEEP BLOOD AGAR receive FDA 510(k) clearance?

SHEEP BLOOD AGAR received FDA 510(k) clearance on 1984-05-31, under 510(k) number K841748.

Who is the listed applicant for SHEEP BLOOD AGAR?

The FDA 510(k) record lists The Montana Deaconess Medical Center as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SHEEP BLOOD AGAR?

The FDA product code for SHEEP BLOOD AGAR is KZI.

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Other records listing The Montana Deaconess Medical Center 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.

K841752XYLOSE-LYSINE DESOXYCHOLATE AGARK841753MACCONKEY AGARK841747MANNITOL SALT AGARK841750MARTIN-LEWIS AGARK841751LEVINE EOSIN METHYLENE BLUE AGARK841749CHOCOLATE AGAR

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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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