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FDA 510(k)

LANCER GLYCOSYLATED HEMOGLOBIN

K-Number: K810638 · 1981-05-08

ApplicantSherwood Medical Co.
Decision Date1981-05-08
Product CodeLCP
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

LANCER GLYCOSYLATED HEMOGLOBIN is the device name listed in this FDA 510(k) record. The listed applicant is Sherwood Medical Co.. It received FDA 510(k) clearance on 1981-05-08 under 510(k) number K810638. 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 LANCER GLYCOSYLATED HEMOGLOBIN?

LANCER GLYCOSYLATED HEMOGLOBIN is a medical device that received FDA 510(k) clearance on 1981-05-08. The listed applicant is Sherwood Medical Co.. The 510(k) number is K810638.

When did LANCER GLYCOSYLATED HEMOGLOBIN receive FDA 510(k) clearance?

LANCER GLYCOSYLATED HEMOGLOBIN received FDA 510(k) clearance on 1981-05-08, under 510(k) number K810638.

Who is the listed applicant for LANCER GLYCOSYLATED HEMOGLOBIN?

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

What is the FDA product code for LANCER GLYCOSYLATED HEMOGLOBIN?

The FDA product code for LANCER GLYCOSYLATED 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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