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FDA 510(k)

CULTURE MEDIUM FOR PATHOGENIC NEISSER

K-Number: K841833 · 1984-05-14

ApplicantMicroline Scientific
Decision Date1984-05-14
Product CodeJTY
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

CULTURE MEDIUM FOR PATHOGENIC NEISSER is the device name listed in this FDA 510(k) record. The listed applicant is Microline Scientific. It received FDA 510(k) clearance on 1984-05-14 under 510(k) number K841833. The device is classified under product code JTY. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CULTURE MEDIUM FOR PATHOGENIC NEISSER?

CULTURE MEDIUM FOR PATHOGENIC NEISSER is a medical device that received FDA 510(k) clearance on 1984-05-14. The listed applicant is Microline Scientific. The 510(k) number is K841833.

When did CULTURE MEDIUM FOR PATHOGENIC NEISSER receive FDA 510(k) clearance?

CULTURE MEDIUM FOR PATHOGENIC NEISSER received FDA 510(k) clearance on 1984-05-14, under 510(k) number K841833.

Who is the listed applicant for CULTURE MEDIUM FOR PATHOGENIC NEISSER?

The FDA 510(k) record lists Microline Scientific as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CULTURE MEDIUM FOR PATHOGENIC NEISSER?

The FDA product code for CULTURE MEDIUM FOR PATHOGENIC NEISSER is JTY.

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Other records listing Microline Scientific 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.

K841845SELECTIVE CULTURE MED. COLUMBIA CNAK841586CHOCOLATE AGARK841844DIFFERENTIAL CULTURE MEDIUM-BIGGY AGARK841842DIFFERENTIAL CULTURE MED. MACCONKEY AGARK841843DIFFERENTIAL CULTURE MED. LEVINE EMBK841840SELECTIVE CULTURE MED. PHENYLETHYL ALCO

View all 14 devices →

Related Devices (Code: JTY)

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.

K210511InTray GCBiomed Diagnostics IncorporatedK993033INTRAY GCBiomed Diagnostics, Inc.K954986GC BASE W/ 1% GCHIRemel, L.P.K950196CULTURE MEDIA, FOR ISOLATION OF PATHOGENIC NEISSERIABioclinical Systems, Inc.K933122MICROBIOLOGICAL CULTURE MEDIA,MARTIN LEWIS AGARBioclinical Systems, Inc.K933121MICROBIOLOGICAL CULTURE MEDIA,CHOCOLATE AGARBioclinical Systems, 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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