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FDA 510(k)

MIS ELECTROSURGICAL ELECTRODES

K-Number: K940192 · 1994-04-19

ApplicantNational Wire & Stamping, Inc.
Decision Date1994-04-19
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MIS ELECTROSURGICAL ELECTRODES is the device name listed in this FDA 510(k) record. The listed applicant is National Wire & Stamping, Inc.. It received FDA 510(k) clearance on 1994-04-19 under 510(k) number K940192. 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 MIS ELECTROSURGICAL ELECTRODES?

MIS ELECTROSURGICAL ELECTRODES is a medical device that received FDA 510(k) clearance on 1994-04-19. The listed applicant is National Wire & Stamping, Inc.. The 510(k) number is K940192.

When did MIS ELECTROSURGICAL ELECTRODES receive FDA 510(k) clearance?

MIS ELECTROSURGICAL ELECTRODES received FDA 510(k) clearance on 1994-04-19, under 510(k) number K940192.

Who is the listed applicant for MIS ELECTROSURGICAL ELECTRODES?

The FDA 510(k) record lists National Wire & Stamping, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MIS ELECTROSURGICAL ELECTRODES?

The FDA product code for MIS ELECTROSURGICAL ELECTRODES is GEI.

Related Clinical Trials

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.

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Other records listing National Wire & Stamping, 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.

K940191ELECTROSURGICAL LOOP ELECTRODEK861495ELECTROSURGICAL BLADE ELECTRODE (SOLID TYPE)K861595BALL ELECTRODESK861594ELECTROSURGICAL NEEDLE ELECTRODE (SOLID TYPE)

Related Devices (Code: GEI)

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.

K261959Neptune® SafeAir® 10ft Smoke Evacuation Pencil, Square Coated, 70mm Blade, Push Button Switch (0703-046-100);Neptune® SafeAir® 10ft Smoke Evacuation Pencil, Square Coated, Push Button Switch, Bulk Non-Sterile (0703-046-102);Neptune® SafeAir® 10ft Smoke Evacuation Pencil, Square Coated, 70mm Blade, Rocker Switch (0703-047-100);Neptune® SafeAir® 10ft Smoke Evacuation Pencil, Square Coated, Rocker Switch, Bulk Non-Sterile (0703-047-102)Stryker InstrumentsK254196HARMONIC 1100 Shears (HAR1120); HARMONIC 1100 Shears (HAR1136)Ethicon Endo-Surgery, LLCK261070LigaSure™ RAS Maryland Jaw Vessel Sealer/Divider, Nano-coatedCovidien, LLCK254185Potenza PrimeJeisys Medical IncorporatedK262364Ellian Enigma RF DeviceEllian CorpK253859Scarlet Pro (Scarlet Pro)VIOL Co., Ltd.

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.

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