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FDA 510(k)

GLEESON CLOT-BUSTER

K-Number: K920139 · 1992-04-15

ApplicantConmedcorp
Decision Date1992-04-15
Product CodeGCI
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

GLEESON CLOT-BUSTER is the device name listed in this FDA 510(k) record. The listed applicant is Conmedcorp. It received FDA 510(k) clearance on 1992-04-15 under 510(k) number K920139. The device is classified under product code GCI. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GLEESON CLOT-BUSTER?

GLEESON CLOT-BUSTER is a medical device that received FDA 510(k) clearance on 1992-04-15. The listed applicant is Conmedcorp. The 510(k) number is K920139.

When did GLEESON CLOT-BUSTER receive FDA 510(k) clearance?

GLEESON CLOT-BUSTER received FDA 510(k) clearance on 1992-04-15, under 510(k) number K920139.

Who is the listed applicant for GLEESON CLOT-BUSTER?

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

What is the FDA product code for GLEESON CLOT-BUSTER?

The FDA product code for GLEESON CLOT-BUSTER is GCI.

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Other records listing Conmedcorp as applicant

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Related Devices (Code: GCI)

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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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