FDA 510(k)

MICRODISCECTOMY CURETTE SET

K-Number: K875292 · 1988-01-29

ApplicantT. Korossurgical Instruments Corp.

Decision Date1988-01-29

Product CodeFZS

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

MICRODISCECTOMY CURETTE SET 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 1988-01-29 under 510(k) number K875292. The device is classified under product code FZS. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICRODISCECTOMY CURETTE SET?

MICRODISCECTOMY CURETTE SET is a medical device that received FDA 510(k) clearance on 1988-01-29. The listed applicant is T. Korossurgical Instruments Corp.. The 510(k) number is K875292.

When did MICRODISCECTOMY CURETTE SET receive FDA 510(k) clearance?

MICRODISCECTOMY CURETTE SET received FDA 510(k) clearance on 1988-01-29, under 510(k) number K875292.

Who is the listed applicant for MICRODISCECTOMY CURETTE SET?

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 MICRODISCECTOMY CURETTE SET?

The FDA product code for MICRODISCECTOMY CURETTE SET is FZS.

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Other records listing T. Korossurgical Instruments Corp. as applicant

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Related Devices (Code: FZS)

K932493SURGICAL CURETTEWhitney Products, Inc.K902000KEVTEK(TM) LASER DRAPE/ORGAN PROTECTOR/EYE SHIELDKevtek Medical Products, Inc.K892521CYMED MICROSKIN(R) DISPOSABLE IRRIGATION SLEEVECymed, Inc.K891888CURRETTES - PIFFARD, WOLF, VIDAL-SCRAPERZinnanti Surgical Instruments, Inc.K891334ACU-CURETTEAcuderm, Inc.K890366ADENOID CURETTEKinetic Medical Products

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.