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FDA 510(k)

LANCER COAGENT PT KIT

K-Number: K792031 · 1979-11-05

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

Device Summary

LANCER COAGENT PT 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 K792031. The device is classified under product code GJS. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LANCER COAGENT PT KIT?

LANCER COAGENT PT 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 K792031.

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

LANCER COAGENT PT KIT received FDA 510(k) clearance on 1979-11-05, under 510(k) number K792031.

Who is the listed applicant for LANCER COAGENT PT 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 PT KIT?

The FDA product code for LANCER COAGENT PT KIT is GJS.

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Other records listing Sherwood Medical Co. as applicant

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Related Devices (Code: GJS)

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.

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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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