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FDA 510(k)

CULTURIA MACCONKEY/CLED #DM87

K-Number: K800215 · 1980-02-13

ApplicantClinical Convenience Products, Inc.
Decision Date1980-02-13
Product CodeJXA
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

CULTURIA MACCONKEY/CLED #DM87 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 1980-02-13 under 510(k) number K800215. 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/CLED #DM87?

CULTURIA MACCONKEY/CLED #DM87 is a medical device that received FDA 510(k) clearance on 1980-02-13. The listed applicant is Clinical Convenience Products, Inc.. The 510(k) number is K800215.

When did CULTURIA MACCONKEY/CLED #DM87 receive FDA 510(k) clearance?

CULTURIA MACCONKEY/CLED #DM87 received FDA 510(k) clearance on 1980-02-13, under 510(k) number K800215.

Who is the listed applicant for CULTURIA MACCONKEY/CLED #DM87?

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/CLED #DM87?

The FDA product code for CULTURIA MACCONKEY/CLED #DM87 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 SYSTEMSK792579CULTURIA MACCONKEY/COLUMBIA CNAK792284CULTURIA 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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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