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FDA 510(k)

COAGULATOR CUTTER, ENDOSCOPIC BIPOLAR AND ACCESSORIES

K-Number: K943776 · 1994-11-03

ApplicantRichard Wolf Medical Instruments Corp.
Decision Date1994-11-03
Product CodeHIN
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

COAGULATOR CUTTER, ENDOSCOPIC BIPOLAR AND ACCESSORIES is the device name listed in this FDA 510(k) record. The listed applicant is Richard Wolf Medical Instruments Corp.. It received FDA 510(k) clearance on 1994-11-03 under 510(k) number K943776. The device is classified under product code HIN. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COAGULATOR CUTTER, ENDOSCOPIC BIPOLAR AND ACCESSORIES?

COAGULATOR CUTTER, ENDOSCOPIC BIPOLAR AND ACCESSORIES is a medical device that received FDA 510(k) clearance on 1994-11-03. The listed applicant is Richard Wolf Medical Instruments Corp.. The 510(k) number is K943776.

When did COAGULATOR CUTTER, ENDOSCOPIC BIPOLAR AND ACCESSORIES receive FDA 510(k) clearance?

COAGULATOR CUTTER, ENDOSCOPIC BIPOLAR AND ACCESSORIES received FDA 510(k) clearance on 1994-11-03, under 510(k) number K943776.

Who is the listed applicant for COAGULATOR CUTTER, ENDOSCOPIC BIPOLAR AND ACCESSORIES?

The FDA 510(k) record lists Richard Wolf Medical Instruments Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for COAGULATOR CUTTER, ENDOSCOPIC BIPOLAR AND ACCESSORIES?

The FDA product code for COAGULATOR CUTTER, ENDOSCOPIC BIPOLAR AND ACCESSORIES is HIN.

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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.

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