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FDA 510(k)

BAYONET FORCEPS BIPOLAR IRRIGATING

K-Number: K002752 · 2000-11-20

ApplicantQ2 Medical
Decision Date2000-11-20
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

BAYONET FORCEPS BIPOLAR IRRIGATING is the device name listed in this FDA 510(k) record. The listed applicant is Q2 Medical. It received FDA 510(k) clearance on 2000-11-20 under 510(k) number K002752. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BAYONET FORCEPS BIPOLAR IRRIGATING?

BAYONET FORCEPS BIPOLAR IRRIGATING is a medical device that received FDA 510(k) clearance on 2000-11-20. The listed applicant is Q2 Medical. The 510(k) number is K002752.

When did BAYONET FORCEPS BIPOLAR IRRIGATING receive FDA 510(k) clearance?

BAYONET FORCEPS BIPOLAR IRRIGATING received FDA 510(k) clearance on 2000-11-20, under 510(k) number K002752.

Who is the listed applicant for BAYONET FORCEPS BIPOLAR IRRIGATING?

The FDA 510(k) record lists Q2 Medical as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BAYONET FORCEPS BIPOLAR IRRIGATING?

The FDA product code for BAYONET FORCEPS BIPOLAR IRRIGATING is GEI.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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