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FDA 510(k)

LANCER COAGENT APTT KIT

K-Number: K792048 · 1979-11-05

ApplicantSherwood Medical Co.
Decision Date1979-11-05
Product CodeGGW
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

LANCER COAGENT APTT KIT 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 1979-11-05 under 510(k) number K792048. The device is classified under product code GGW. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LANCER COAGENT APTT KIT?

LANCER COAGENT APTT KIT is a medical device that received FDA 510(k) clearance on 1979-11-05. The listed applicant is Sherwood Medical Co.. The 510(k) number is K792048.

When did LANCER COAGENT APTT KIT receive FDA 510(k) clearance?

LANCER COAGENT APTT KIT received FDA 510(k) clearance on 1979-11-05, under 510(k) number K792048.

Who is the listed applicant for LANCER COAGENT APTT KIT?

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 COAGENT APTT KIT?

The FDA product code for LANCER COAGENT APTT KIT is GGW.

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Other records listing Sherwood Medical Co. as applicant

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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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