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FDA 510(k)

CULTURIA MACCONKEY/COLUMBIA CNA

K-Number: K792579 · 1980-01-11

ApplicantClinical Convenience Products, Inc.
Decision Date1980-01-11
Product CodeJXA
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

CULTURIA MACCONKEY/COLUMBIA CNA is the device name listed in this FDA 510(k) record. The listed applicant is Clinical Convenience Products, Inc.. It received FDA 510(k) clearance on 1980-01-11 under 510(k) number K792579. The device is classified under product code JXA. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CULTURIA MACCONKEY/COLUMBIA CNA?

CULTURIA MACCONKEY/COLUMBIA CNA is a medical device that received FDA 510(k) clearance on 1980-01-11. The listed applicant is Clinical Convenience Products, Inc.. The 510(k) number is K792579.

When did CULTURIA MACCONKEY/COLUMBIA CNA receive FDA 510(k) clearance?

CULTURIA MACCONKEY/COLUMBIA CNA received FDA 510(k) clearance on 1980-01-11, under 510(k) number K792579.

Who is the listed applicant for CULTURIA MACCONKEY/COLUMBIA CNA?

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

What is the FDA product code for CULTURIA MACCONKEY/COLUMBIA CNA?

The FDA product code for CULTURIA MACCONKEY/COLUMBIA CNA is JXA.

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Other records listing Clinical Convenience Products, 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.

K934759CULTURIA MACCONKEY-MUGK870502CULTURIA MACCONKEY-MUG/MODIFIED TSA SYSTEMSK864764CULTURIA MACCONKEY-MUG/CLED SYSTEMSK800215CULTURIA MACCONKEY/CLED #DM87K792284CULTURIA EMB/COLUMBIA CNA W/5% SHEEP

Related Devices (Code: JXA)

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.

K011043OSMETECH MICROBIAL ANALYSER-URINARY TRACT INFECTION DETECTOR (OMA-UTI)OsmetechK981084URISCREENDiatech Diagnostics,Inc.K972676URINE SCREENING DEVICECombact Diagnostic Systems , Ltd.K952246TRI-TECHIN. CUSTOM BLOOD AND/OR URINE TRANSPORT KITTri-Tech, Inc.K950257MULTIPLE (IZON DBS & URINE COLLECTION KIT)Izon Business Products, Inc.K950246MULTIPLE (IZON URINE COLLECTION KIT)Izon Business Products, 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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