FDA 510(k)

ROTO FIT BIOPSY FORCEPS

K-Number: K926527 · 1994-02-25

Decision Date1994-02-25

Product CodeHFB

Advisory CommitteeOB

DecisionSubstantially Equivalent

Device Summary

ROTO FIT BIOPSY FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Thomasville Medical Assoc.. It received FDA 510(k) clearance on 1994-02-25 under 510(k) number K926527. The device is classified under product code HFB. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ROTO FIT BIOPSY FORCEPS?

ROTO FIT BIOPSY FORCEPS is a medical device that received FDA 510(k) clearance on 1994-02-25. The listed applicant is Thomasville Medical Assoc.. The 510(k) number is K926527.

When did ROTO FIT BIOPSY FORCEPS receive FDA 510(k) clearance?

ROTO FIT BIOPSY FORCEPS received FDA 510(k) clearance on 1994-02-25, under 510(k) number K926527.

Who is the listed applicant for ROTO FIT BIOPSY FORCEPS?

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

What is the FDA product code for ROTO FIT BIOPSY FORCEPS?

The FDA product code for ROTO FIT BIOPSY FORCEPS is HFB.

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Other records listing Thomasville Medical Assoc. as applicant

K926429VAGINAL SPECULA: CUSCO, GUTTMAN, INFANT K926535GOMCO CIRCUMCISION CLAMP K926471MOGAN CIRCUMCISION CLAMP K926531HYSTERECTOMY FORCEPS K926532ENDO CERVICAL CURETTE K930030SUCTION TUBES: HOUSE, BARON

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Related Devices (Code: HFB)

K011488SPIRABRUSH CX BIOPSY INSTRUMENTTrylon Corp.K944444CIT BIOPSY PUNCHESChirurgische Instrumente K930773SYMBIOSIS GYNECOLOGICAL BIOPSY FORCEPSSymbiosis Corp.K933767FORCEPS, BIOPSY GYNECOLOGICAL INSTRU/BIOPSYMahe-Medizintechnik K926595OWENS BIOPSY FORCEPSOwens Industries, Inc.K930036THOMAS MEDICAL BIOPSY FORCEPSThomasville Medical Assoc.

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.