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FDA 510(k)

REPLACEABLE BATTERY PERFECTEMP 2 CAUT

K-Number: K812644 · 1981-10-26

ApplicantKey Medical, Inc.
Decision Date1981-10-26
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

REPLACEABLE BATTERY PERFECTEMP 2 CAUT is the device name listed in this FDA 510(k) record. The listed applicant is Key Medical, Inc.. It received FDA 510(k) clearance on 1981-10-26 under 510(k) number K812644. 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 REPLACEABLE BATTERY PERFECTEMP 2 CAUT?

REPLACEABLE BATTERY PERFECTEMP 2 CAUT is a medical device that received FDA 510(k) clearance on 1981-10-26. The listed applicant is Key Medical, Inc.. The 510(k) number is K812644.

When did REPLACEABLE BATTERY PERFECTEMP 2 CAUT receive FDA 510(k) clearance?

REPLACEABLE BATTERY PERFECTEMP 2 CAUT received FDA 510(k) clearance on 1981-10-26, under 510(k) number K812644.

Who is the listed applicant for REPLACEABLE BATTERY PERFECTEMP 2 CAUT?

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

What is the FDA product code for REPLACEABLE BATTERY PERFECTEMP 2 CAUT?

The FDA product code for REPLACEABLE BATTERY PERFECTEMP 2 CAUT 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 Key Medical, 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.

K821127KEY DRILLK812760HI-TEMP CARDIOVASCULAR CAUTERYK810909MICRO CAUTERY

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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