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FDA 510(k)

UNIPOWER RECHARGEABLE BATTERY PACK

K-Number: K940842 · 1994-09-07

ApplicantUnipower Corp.
Decision Date1994-09-07
Product CodeLDD
Advisory CommitteeCV
DecisionSubstantially Equivalent - Subject to Tracking Reg.

Device Summary

UNIPOWER RECHARGEABLE BATTERY PACK is the device name listed in this FDA 510(k) record. The listed applicant is Unipower Corp.. It received FDA 510(k) clearance on 1994-09-07 under 510(k) number K940842. The device is classified under product code LDD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent - Subject to Tracking Reg..

Frequently Asked Questions

What is the UNIPOWER RECHARGEABLE BATTERY PACK?

UNIPOWER RECHARGEABLE BATTERY PACK is a medical device that received FDA 510(k) clearance on 1994-09-07. The listed applicant is Unipower Corp.. The 510(k) number is K940842.

When did UNIPOWER RECHARGEABLE BATTERY PACK receive FDA 510(k) clearance?

UNIPOWER RECHARGEABLE BATTERY PACK received FDA 510(k) clearance on 1994-09-07, under 510(k) number K940842.

Who is the listed applicant for UNIPOWER RECHARGEABLE BATTERY PACK?

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

What is the FDA product code for UNIPOWER RECHARGEABLE BATTERY PACK?

The FDA product code for UNIPOWER RECHARGEABLE BATTERY PACK is LDD.

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 Unipower Corp. 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.

K936141UNIPOWER RECHARGEABLE BATTERY PACKK935111UNIPOWERR RECHARGEABLE BATTERY PACK

Related Devices (Code: LDD)

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.

K203231Switched Internal PaddlesPhilips North America, LLCK200849Tempus LS - ManualRemote Diagnostic Technologies, Ltd. A Philips CompanyK182503Sterilizable Internal Defibrillation Paddles for use with LIFEPAK defibrillators/monitorsPhysio-Control, Inc.K103651CARDIOMEDCardio Medical Products, Inc.K103783EURO DEFI PADS ADULT; EURO DEFI PADS ADULT RADIOTRANSPARENT: EURO DEFI PADS PEDIATRICFiab SpaK103334CARDIO MEDCardio Medical Products, Inc.

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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