FDA 510(k)

ARTHROSCOPY SUCTION BIOPSY PUNCH

K-Number: K850527 · 1985-03-14

ApplicantT. Korossurgical Instruments Corp.

Decision Date1985-03-14

Product CodeHTZ

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

ARTHROSCOPY SUCTION BIOPSY PUNCH is the device name listed in this FDA 510(k) record. The listed applicant is T. Korossurgical Instruments Corp.. It received FDA 510(k) clearance on 1985-03-14 under 510(k) number K850527. The device is classified under product code HTZ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARTHROSCOPY SUCTION BIOPSY PUNCH?

ARTHROSCOPY SUCTION BIOPSY PUNCH is a medical device that received FDA 510(k) clearance on 1985-03-14. The listed applicant is T. Korossurgical Instruments Corp.. The 510(k) number is K850527.

When did ARTHROSCOPY SUCTION BIOPSY PUNCH receive FDA 510(k) clearance?

ARTHROSCOPY SUCTION BIOPSY PUNCH received FDA 510(k) clearance on 1985-03-14, under 510(k) number K850527.

Who is the listed applicant for ARTHROSCOPY SUCTION BIOPSY PUNCH?

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

What is the FDA product code for ARTHROSCOPY SUCTION BIOPSY PUNCH?

The FDA product code for ARTHROSCOPY SUCTION BIOPSY PUNCH is HTZ.

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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.