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FDA 510(k)

FORCEPS, BIOPSY GYNECOLOGICAL INSTRU/BIOPSY

K-Number: K933767 · 1994-05-26

ApplicantMahe-Medizintechnik
Decision Date1994-05-26
Product CodeHFB
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

FORCEPS, BIOPSY GYNECOLOGICAL INSTRU/BIOPSY is the device name listed in this FDA 510(k) record. The listed applicant is Mahe-Medizintechnik. It received FDA 510(k) clearance on 1994-05-26 under 510(k) number K933767. 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 FORCEPS, BIOPSY GYNECOLOGICAL INSTRU/BIOPSY?

FORCEPS, BIOPSY GYNECOLOGICAL INSTRU/BIOPSY is a medical device that received FDA 510(k) clearance on 1994-05-26. The listed applicant is Mahe-Medizintechnik. The 510(k) number is K933767.

When did FORCEPS, BIOPSY GYNECOLOGICAL INSTRU/BIOPSY receive FDA 510(k) clearance?

FORCEPS, BIOPSY GYNECOLOGICAL INSTRU/BIOPSY received FDA 510(k) clearance on 1994-05-26, under 510(k) number K933767.

Who is the listed applicant for FORCEPS, BIOPSY GYNECOLOGICAL INSTRU/BIOPSY?

The FDA 510(k) record lists Mahe-Medizintechnik as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FORCEPS, BIOPSY GYNECOLOGICAL INSTRU/BIOPSY?

The FDA product code for FORCEPS, BIOPSY GYNECOLOGICAL INSTRU/BIOPSY is HFB.

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Other records listing Mahe-Medizintechnik 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.

K942821MAHE INSTRUMENTSK942819TROCAR WITH SHIELDK933768COAGULATOR, LAPAROSCOPIC, LUNIPOLAR/ACCESSORIESK933770FORCEPS, ENT INSTR, ENT MANUAL SURG RETRACT/ALL TYPEK935442MAHE INSTRUMENTSK933772PUNCH SURGICAL

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Related Devices (Code: HFB)

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.

K011488SPIRABRUSH CX BIOPSY INSTRUMENTTrylon Corp.K944444CIT BIOPSY PUNCHESChirurgische InstrumenteK930773SYMBIOSIS GYNECOLOGICAL BIOPSY FORCEPSSymbiosis Corp.K926595OWENS BIOPSY FORCEPSOwens Industries, Inc.K926527ROTO FIT BIOPSY FORCEPSThomasville Medical Assoc.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.

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