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FDA 510(k)

GLYCO-SEP/ALC TEST KIT FOR SEPARAT OF HEMOGLOBIN

K-Number: K852986 · 1985-08-19

ApplicantClinical Technology Corp.
Decision Date1985-08-19
Product CodeLCP
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

GLYCO-SEP/ALC TEST KIT FOR SEPARAT OF HEMOGLOBIN is the device name listed in this FDA 510(k) record. The listed applicant is Clinical Technology Corp.. It received FDA 510(k) clearance on 1985-08-19 under 510(k) number K852986. The device is classified under product code LCP. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GLYCO-SEP/ALC TEST KIT FOR SEPARAT OF HEMOGLOBIN?

GLYCO-SEP/ALC TEST KIT FOR SEPARAT OF HEMOGLOBIN is a medical device that received FDA 510(k) clearance on 1985-08-19. The listed applicant is Clinical Technology Corp.. The 510(k) number is K852986.

When did GLYCO-SEP/ALC TEST KIT FOR SEPARAT OF HEMOGLOBIN receive FDA 510(k) clearance?

GLYCO-SEP/ALC TEST KIT FOR SEPARAT OF HEMOGLOBIN received FDA 510(k) clearance on 1985-08-19, under 510(k) number K852986.

Who is the listed applicant for GLYCO-SEP/ALC TEST KIT FOR SEPARAT OF HEMOGLOBIN?

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

What is the FDA product code for GLYCO-SEP/ALC TEST KIT FOR SEPARAT OF HEMOGLOBIN?

The FDA product code for GLYCO-SEP/ALC TEST KIT FOR SEPARAT OF HEMOGLOBIN is LCP.

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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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