FDA 510(k)

KEVORKIAN-YOUNGE BIOPSY PUNCH, #90-6610

K-Number: K802457 · 1981-01-12

Decision Date1981-01-12

Product CodeHFB

Advisory CommitteeOB

DecisionSubstantially Equivalent

Device Summary

KEVORKIAN-YOUNGE BIOPSY PUNCH, #90-6610 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 K802457. 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 PUNCH, #90-6610?

KEVORKIAN-YOUNGE BIOPSY PUNCH, #90-6610 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 K802457.

When did KEVORKIAN-YOUNGE BIOPSY PUNCH, #90-6610 receive FDA 510(k) clearance?

KEVORKIAN-YOUNGE BIOPSY PUNCH, #90-6610 received FDA 510(k) clearance on 1981-01-12, under 510(k) number K802457.

Who is the listed applicant for KEVORKIAN-YOUNGE BIOPSY PUNCH, #90-6610?

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 PUNCH, #90-6610?

The FDA product code for KEVORKIAN-YOUNGE BIOPSY PUNCH, #90-6610 is HFB.

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

K843693JACOBS HIGH VACUUM SUCTION UNIT 05-2570 K842112TISCHLER CERVICAL BIOPSY PUNCH FORCEPS K842111KOGAN ENDOSPECULUM 9-1/2 K822448SCISSORS, VARIOUS K802458KEVORKIAN-YOUNGE BIOPSY CURETTE #90-6611 K801273MAGILL CATHETER INTRO. FORCEPS

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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.