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FDA 510(k)

YESNG RESUABLE BIPOLAR FORCEPS

K-Number: K881407 · 1988-04-14

ApplicantFerguson Medical
Decision Date1988-04-14
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

YESNG RESUABLE BIPOLAR FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Ferguson Medical. It received FDA 510(k) clearance on 1988-04-14 under 510(k) number K881407. 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 YESNG RESUABLE BIPOLAR FORCEPS?

YESNG RESUABLE BIPOLAR FORCEPS is a medical device that received FDA 510(k) clearance on 1988-04-14. The listed applicant is Ferguson Medical. The 510(k) number is K881407.

When did YESNG RESUABLE BIPOLAR FORCEPS receive FDA 510(k) clearance?

YESNG RESUABLE BIPOLAR FORCEPS received FDA 510(k) clearance on 1988-04-14, under 510(k) number K881407.

Who is the listed applicant for YESNG RESUABLE BIPOLAR FORCEPS?

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

What is the FDA product code for YESNG RESUABLE BIPOLAR FORCEPS?

The FDA product code for YESNG RESUABLE BIPOLAR FORCEPS is GEI.

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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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