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FDA 510(k)

BATTERY PACK #1012NC

K-Number: K931266 · 1994-02-03

ApplicantPortable Power Systems, Inc.
Decision Date1994-02-03
Product CodeLDD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

BATTERY PACK #1012NC is the device name listed in this FDA 510(k) record. The listed applicant is Portable Power Systems, Inc.. It received FDA 510(k) clearance on 1994-02-03 under 510(k) number K931266. The device is classified under product code LDD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BATTERY PACK #1012NC?

BATTERY PACK #1012NC is a medical device that received FDA 510(k) clearance on 1994-02-03. The listed applicant is Portable Power Systems, Inc.. The 510(k) number is K931266.

When did BATTERY PACK #1012NC receive FDA 510(k) clearance?

BATTERY PACK #1012NC received FDA 510(k) clearance on 1994-02-03, under 510(k) number K931266.

Who is the listed applicant for BATTERY PACK #1012NC?

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

What is the FDA product code for BATTERY PACK #1012NC?

The FDA product code for BATTERY PACK #1012NC 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 Portable Power Systems, 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.

K970234SEALED LEAD ACID BATTERY PACKK946080PHYSIO CONTROL LIFEPAK 200 AUTO DEFIBRILLATORK945043BATTERY PACK #PMX120-18AK931483REPLACEMENT BATERY FOR GE AMX-4 PORT. X-RAY MACH.K934439RECHARGEABLE BATTERY PACK FOR CRITIKON 8100 VITAL SIGNS MONITORK934508BATTERY PACK# S1024NC

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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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