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FDA 510(k)

CULTURE MEDIA NONSELECTIVE & NONDIFFERENTIAL

K-Number: K850724 · 1985-03-25

ApplicantRapid City Regional Hospital, Inc.
Decision Date1985-03-25
Product CodeKZI
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

CULTURE MEDIA NONSELECTIVE & NONDIFFERENTIAL is the device name listed in this FDA 510(k) record. The listed applicant is Rapid City Regional Hospital, Inc.. It received FDA 510(k) clearance on 1985-03-25 under 510(k) number K850724. 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 CULTURE MEDIA NONSELECTIVE & NONDIFFERENTIAL?

CULTURE MEDIA NONSELECTIVE & NONDIFFERENTIAL is a medical device that received FDA 510(k) clearance on 1985-03-25. The listed applicant is Rapid City Regional Hospital, Inc.. The 510(k) number is K850724.

When did CULTURE MEDIA NONSELECTIVE & NONDIFFERENTIAL receive FDA 510(k) clearance?

CULTURE MEDIA NONSELECTIVE & NONDIFFERENTIAL received FDA 510(k) clearance on 1985-03-25, under 510(k) number K850724.

Who is the listed applicant for CULTURE MEDIA NONSELECTIVE & NONDIFFERENTIAL?

The FDA 510(k) record lists Rapid City Regional Hospital, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CULTURE MEDIA NONSELECTIVE & NONDIFFERENTIAL?

The FDA product code for CULTURE MEDIA NONSELECTIVE & NONDIFFERENTIAL is KZI.

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Other records listing Rapid City Regional Hospital, 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.

K850719DNASE TEST MEDIA, CHRISTENSEN'S UREA AGARK850716SELENITE F BROTHK850720EOSIN METHYLENE BLUE AGAR, SS AGAR, XLD AGAR 6.5%K850722MARTIN LEWIS AGARK850717AMIES TRANSPORT MEDIAK850721KLIGER'S IRON AGAR, SIM MEDIA, MRVP MEDIUM, BILE E

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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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