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FDA 510(k)

KEVORKIAN-YOUNGE BIOPSY CURETTE #90-6611

K-Number: K802458 · 1981-01-12

ApplicantJ. Sklar Mfg. Co., Inc.
Decision Date1981-01-12
Product CodeHFB
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

KEVORKIAN-YOUNGE BIOPSY CURETTE #90-6611 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 1981-01-12 under 510(k) number K802458. 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 KEVORKIAN-YOUNGE BIOPSY CURETTE #90-6611?

KEVORKIAN-YOUNGE BIOPSY CURETTE #90-6611 is a medical device that received FDA 510(k) clearance on 1981-01-12. The listed applicant is J. Sklar Mfg. Co., Inc.. The 510(k) number is K802458.

When did KEVORKIAN-YOUNGE BIOPSY CURETTE #90-6611 receive FDA 510(k) clearance?

KEVORKIAN-YOUNGE BIOPSY CURETTE #90-6611 received FDA 510(k) clearance on 1981-01-12, under 510(k) number K802458.

Who is the listed applicant for KEVORKIAN-YOUNGE BIOPSY CURETTE #90-6611?

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 KEVORKIAN-YOUNGE BIOPSY CURETTE #90-6611?

The FDA product code for KEVORKIAN-YOUNGE BIOPSY CURETTE #90-6611 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 05-2570K842112TISCHLER CERVICAL BIOPSY PUNCH FORCEPSK842111KOGAN ENDOSPECULUM 9-1/2K822448SCISSORS, VARIOUSK802457KEVORKIAN-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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