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FDA 510(k)

OLYMPUS DISPOSABLE BIOPSY FORCEPS

K-Number: K930241 · 1993-04-20

ApplicantOlympus Corp.
Decision Date1993-04-20
Product CodeKNW
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

OLYMPUS DISPOSABLE BIOPSY FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Olympus Corp.. It received FDA 510(k) clearance on 1993-04-20 under 510(k) number K930241. 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 OLYMPUS DISPOSABLE BIOPSY FORCEPS?

OLYMPUS DISPOSABLE BIOPSY FORCEPS is a medical device that received FDA 510(k) clearance on 1993-04-20. The listed applicant is Olympus Corp.. The 510(k) number is K930241.

When did OLYMPUS DISPOSABLE BIOPSY FORCEPS receive FDA 510(k) clearance?

OLYMPUS DISPOSABLE BIOPSY FORCEPS received FDA 510(k) clearance on 1993-04-20, under 510(k) number K930241.

Who is the listed applicant for OLYMPUS DISPOSABLE BIOPSY FORCEPS?

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

What is the FDA product code for OLYMPUS DISPOSABLE BIOPSY FORCEPS?

The FDA product code for OLYMPUS DISPOSABLE BIOPSY FORCEPS is KNW.

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Other records listing Olympus Corp. as applicant

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Related Devices (Code: KNW)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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