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FDA 510(k)

HEMOSTATIC FORCEPS BRUNS.,GEMINI,SPENCER-WELL,KANT

K-Number: K891401 · 1989-04-06

ApplicantZinnanti Surgical Instruments, Inc.
Decision Date1989-04-06
Product CodeGEN
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

HEMOSTATIC FORCEPS BRUNS.,GEMINI,SPENCER-WELL,KANT is the device name listed in this FDA 510(k) record. The listed applicant is Zinnanti Surgical Instruments, Inc.. It received FDA 510(k) clearance on 1989-04-06 under 510(k) number K891401. The device is classified under product code GEN. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HEMOSTATIC FORCEPS BRUNS.,GEMINI,SPENCER-WELL,KANT?

HEMOSTATIC FORCEPS BRUNS.,GEMINI,SPENCER-WELL,KANT is a medical device that received FDA 510(k) clearance on 1989-04-06. The listed applicant is Zinnanti Surgical Instruments, Inc.. The 510(k) number is K891401.

When did HEMOSTATIC FORCEPS BRUNS.,GEMINI,SPENCER-WELL,KANT receive FDA 510(k) clearance?

HEMOSTATIC FORCEPS BRUNS.,GEMINI,SPENCER-WELL,KANT received FDA 510(k) clearance on 1989-04-06, under 510(k) number K891401.

Who is the listed applicant for HEMOSTATIC FORCEPS BRUNS.,GEMINI,SPENCER-WELL,KANT?

The FDA 510(k) record lists Zinnanti Surgical Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HEMOSTATIC FORCEPS BRUNS.,GEMINI,SPENCER-WELL,KANT?

The FDA product code for HEMOSTATIC FORCEPS BRUNS.,GEMINI,SPENCER-WELL,KANT is GEN.

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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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