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FDA 510(k)

BATTERY PACK# S1024NC

K-Number: K934508 · 1994-02-17

ApplicantPortable Power Systems, Inc.
Decision Date1994-02-17
Product CodeLDD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

BATTERY PACK# S1024NC 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 1994-02-17 under 510(k) number K934508. 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# S1024NC?

BATTERY PACK# S1024NC is a medical device that received FDA 510(k) clearance on 1994-02-17. The listed applicant is Portable Power Systems, Inc.. The 510(k) number is K934508.

When did BATTERY PACK# S1024NC receive FDA 510(k) clearance?

BATTERY PACK# S1024NC received FDA 510(k) clearance on 1994-02-17, under 510(k) number K934508.

Who is the listed applicant for BATTERY PACK# S1024NC?

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# S1024NC?

The FDA product code for BATTERY PACK# S1024NC is LDD.

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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 #PMX120-18AK933065BATTERY PACK# S1009LAK934439RECHARGEABLE BATTERY PACK FOR CRITIKON 8100 VITAL SIGNS MONITORK932823BATTERY PACK# S1018LA FOR IVAC 4000, 4200 VITAL CHECK

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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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