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FDA 510(k)

TISCHLER CERVICAL BIOPSY PUNCH FORCEPS

K-Number: K842112 · 1984-07-03

ApplicantJ. Sklar Mfg. Co., Inc.
Decision Date1984-07-03
Product CodeHFB
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

TISCHLER CERVICAL BIOPSY PUNCH FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is J. Sklar Mfg. Co., Inc.. It received FDA 510(k) clearance on 1984-07-03 under 510(k) number K842112. 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 TISCHLER CERVICAL BIOPSY PUNCH FORCEPS?

TISCHLER CERVICAL BIOPSY PUNCH FORCEPS is a medical device that received FDA 510(k) clearance on 1984-07-03. The listed applicant is J. Sklar Mfg. Co., Inc.. The 510(k) number is K842112.

When did TISCHLER CERVICAL BIOPSY PUNCH FORCEPS receive FDA 510(k) clearance?

TISCHLER CERVICAL BIOPSY PUNCH FORCEPS received FDA 510(k) clearance on 1984-07-03, under 510(k) number K842112.

Who is the listed applicant for TISCHLER CERVICAL BIOPSY PUNCH FORCEPS?

The FDA 510(k) record lists J. Sklar Mfg. Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TISCHLER CERVICAL BIOPSY PUNCH FORCEPS?

The FDA product code for TISCHLER CERVICAL BIOPSY PUNCH FORCEPS is HFB.

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Other records listing J. Sklar Mfg. Co., Inc. 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.

K843693JACOBS HIGH VACUUM SUCTION UNIT 05-2570K842111KOGAN ENDOSPECULUM 9-1/2K822448SCISSORS, VARIOUSK802458KEVORKIAN-YOUNGE BIOPSY CURETTE #90-6611K802457KEVORKIAN-YOUNGE BIOPSY PUNCH, #90-6610K801273MAGILL CATHETER INTRO. FORCEPS

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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.K933767FORCEPS, BIOPSY GYNECOLOGICAL INSTRU/BIOPSYMahe-MedizintechnikK926595OWENS BIOPSY FORCEPSOwens Industries, Inc.K926527ROTO FIT 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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