FDA 510(k)

BIOPSY FORCEPS (NON-RIGID)

K-Number: K901339 · 1990-06-11

Decision Date1990-06-11

Product CodeKNW

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

BIOPSY FORCEPS (NON-RIGID) is the device name listed in this FDA 510(k) record. The listed applicant is Applied Medical Technologies. It received FDA 510(k) clearance on 1990-06-11 under 510(k) number K901339. The device is classified under product code KNW. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BIOPSY FORCEPS (NON-RIGID)?

BIOPSY FORCEPS (NON-RIGID) is a medical device that received FDA 510(k) clearance on 1990-06-11. The listed applicant is Applied Medical Technologies. The 510(k) number is K901339.

When did BIOPSY FORCEPS (NON-RIGID) receive FDA 510(k) clearance?

BIOPSY FORCEPS (NON-RIGID) received FDA 510(k) clearance on 1990-06-11, under 510(k) number K901339.

Who is the listed applicant for BIOPSY FORCEPS (NON-RIGID)?

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

What is the FDA product code for BIOPSY FORCEPS (NON-RIGID)?

The FDA product code for BIOPSY FORCEPS (NON-RIGID) is KNW.

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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.