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FDA 510(k)

ELECTROSURGICAL DEVICE, MODEL 26-2500

K-Number: K935490 · 1994-04-01

ApplicantCameron-Miller, Inc.
Decision Date1994-04-01
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ELECTROSURGICAL DEVICE, MODEL 26-2500 is the device name listed in this FDA 510(k) record. The listed applicant is Cameron-Miller, Inc.. It received FDA 510(k) clearance on 1994-04-01 under 510(k) number K935490. 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 DEVICE, MODEL 26-2500?

ELECTROSURGICAL DEVICE, MODEL 26-2500 is a medical device that received FDA 510(k) clearance on 1994-04-01. The listed applicant is Cameron-Miller, Inc.. The 510(k) number is K935490.

When did ELECTROSURGICAL DEVICE, MODEL 26-2500 receive FDA 510(k) clearance?

ELECTROSURGICAL DEVICE, MODEL 26-2500 received FDA 510(k) clearance on 1994-04-01, under 510(k) number K935490.

Who is the listed applicant for ELECTROSURGICAL DEVICE, MODEL 26-2500?

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

What is the FDA product code for ELECTROSURGICAL DEVICE, MODEL 26-2500?

The FDA product code for ELECTROSURGICAL DEVICE, MODEL 26-2500 is GEI.

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Other records listing Cameron-Miller, 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.

K944775ELECTROSURGICAL UNIT MODEL 26-0335K931541MODEL 26-0375, ELECTROSURGICAL GENERATORK931437MODEL 80-1983, ELECTROSURGICAL GENERATORK854109ELECTROSURGICAL DEVICES, 26-0330,26-335,340 & 0345K853972CAMERON-MILLER MODEL 80-2701, BIPOLAR COAGULATORK833449HAND CONTROLLED PENCIL OR SWITCH HAND

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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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