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FDA 510(k)

SOPHER AND BIERER OVUM FORCEPS

K-Number: K926540 · 1994-02-25

ApplicantThomasville Medical Assoc.
Decision Date1994-02-25
Product CodeHLZ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

SOPHER AND BIERER OVUM 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 K926540. The device is classified under product code HLZ. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SOPHER AND BIERER OVUM FORCEPS?

SOPHER AND BIERER OVUM 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 K926540.

When did SOPHER AND BIERER OVUM FORCEPS receive FDA 510(k) clearance?

SOPHER AND BIERER OVUM FORCEPS received FDA 510(k) clearance on 1994-02-25, under 510(k) number K926540.

Who is the listed applicant for SOPHER AND BIERER OVUM 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 SOPHER AND BIERER OVUM FORCEPS?

The FDA product code for SOPHER AND BIERER OVUM FORCEPS is HLZ.

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Other records listing Thomasville Medical Assoc. as applicant

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.

K926429VAGINAL SPECULA: CUSCO, GUTTMAN, INFANTK926471MOGAN CIRCUMCISION CLAMPK926527ROTO FIT BIOPSY FORCEPSK926535GOMCO CIRCUMCISION CLAMPK926532ENDO CERVICAL CURETTEK926531HYSTERECTOMY FORCEPS

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Related Devices (Code: HLZ)

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.

K253586RM Electrode (RMH 25-01)Retmap, Inc.K232273RM Electrode (RMH 23-01)Retmap, Inc.K961805TOMEY DTL ELECTRODETomey Corporation USAK913239GOLDLENS(TM)Doran Instruments, Inc.K844409DTL ELECTRODESauquoit Industries, Inc.K830557ERG-JET ELECTRODEUniverso S.A.

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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