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FDA 510(k)

ST. MARK'S RECTAL BIOPSY FORCEPS

K-Number: K822401 · 1982-08-27

ApplicantKeymed, Inc.
Decision Date1982-08-27
Product CodeKOA
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ST. MARK'S RECTAL BIOPSY FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Keymed, Inc.. It received FDA 510(k) clearance on 1982-08-27 under 510(k) number K822401. The device is classified under product code KOA. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ST. MARK'S RECTAL BIOPSY FORCEPS?

ST. MARK'S RECTAL BIOPSY FORCEPS is a medical device that received FDA 510(k) clearance on 1982-08-27. The listed applicant is Keymed, Inc.. The 510(k) number is K822401.

When did ST. MARK'S RECTAL BIOPSY FORCEPS receive FDA 510(k) clearance?

ST. MARK'S RECTAL BIOPSY FORCEPS received FDA 510(k) clearance on 1982-08-27, under 510(k) number K822401.

Who is the listed applicant for ST. MARK'S RECTAL BIOPSY FORCEPS?

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

What is the FDA product code for ST. MARK'S RECTAL BIOPSY FORCEPS?

The FDA product code for ST. MARK'S RECTAL BIOPSY FORCEPS is KOA.

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Other records listing Keymed, Inc. as applicant

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Related Devices (Code: KOA)

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.

K182664FiXcisionAgency For Medical Innovations GmbHK950267URETHRAL SUTURE GUIDEApplied Medical ResourcesK932465LI VASECTOMYFemcare , Ltd.K921546VASOVASOSTOMY SETCook Urological, Inc.K931181VESITEC SUTURE PASSERVesitec Medical, Inc.K921304DDV LIGATORNorth American Medical, Inc.

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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