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FDA 510(k)

E2550 REUSABLE HANDSWITCHING PENCIL

K-Number: K942183 · 1994-05-17

ApplicantValleylab, Inc.
Decision Date1994-05-17
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

E2550 REUSABLE HANDSWITCHING PENCIL is the device name listed in this FDA 510(k) record. The listed applicant is Valleylab, Inc.. It received FDA 510(k) clearance on 1994-05-17 under 510(k) number K942183. 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 E2550 REUSABLE HANDSWITCHING PENCIL?

E2550 REUSABLE HANDSWITCHING PENCIL is a medical device that received FDA 510(k) clearance on 1994-05-17. The listed applicant is Valleylab, Inc.. The 510(k) number is K942183.

When did E2550 REUSABLE HANDSWITCHING PENCIL receive FDA 510(k) clearance?

E2550 REUSABLE HANDSWITCHING PENCIL received FDA 510(k) clearance on 1994-05-17, under 510(k) number K942183.

Who is the listed applicant for E2550 REUSABLE HANDSWITCHING PENCIL?

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

What is the FDA product code for E2550 REUSABLE HANDSWITCHING PENCIL?

The FDA product code for E2550 REUSABLE HANDSWITCHING PENCIL is GEI.

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Other records listing Valleylab, Inc. as applicant

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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

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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