FDA 510(k)

ELECTROSURGICAL CUTTING & COAGULATION DEVICE & ACCESSORIES

K-Number: K961097 · 1996-06-03

ApplicantDebusk Knitting Mills, Div. Deroyal Industries

Decision Date1996-06-03

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

ELECTROSURGICAL CUTTING & COAGULATION DEVICE & ACCESSORIES is the device name listed in this FDA 510(k) record. The listed applicant is Debusk Knitting Mills, Div. Deroyal Industries. It received FDA 510(k) clearance on 1996-06-03 under 510(k) number K961097. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELECTROSURGICAL CUTTING & COAGULATION DEVICE & ACCESSORIES?

ELECTROSURGICAL CUTTING & COAGULATION DEVICE & ACCESSORIES is a medical device that received FDA 510(k) clearance on 1996-06-03. The listed applicant is Debusk Knitting Mills, Div. Deroyal Industries. The 510(k) number is K961097.

When did ELECTROSURGICAL CUTTING & COAGULATION DEVICE & ACCESSORIES receive FDA 510(k) clearance?

ELECTROSURGICAL CUTTING & COAGULATION DEVICE & ACCESSORIES received FDA 510(k) clearance on 1996-06-03, under 510(k) number K961097.

Who is the listed applicant for ELECTROSURGICAL CUTTING & COAGULATION DEVICE & ACCESSORIES?

The FDA 510(k) record lists Debusk Knitting Mills, Div. Deroyal Industries as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ELECTROSURGICAL CUTTING & COAGULATION DEVICE & ACCESSORIES?

The FDA product code for ELECTROSURGICAL CUTTING & COAGULATION DEVICE & ACCESSORIES is GEI.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.