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FDA 510(k)

REPLACEMENT BATTER FOR ABBOTT LABS LIFECARE 4100 S

K-Number: K931484 · 1994-02-17

ApplicantPortable Power Systems, Inc.
Decision Date1994-02-17
Product CodeBZD
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

REPLACEMENT BATTER FOR ABBOTT LABS LIFECARE 4100 S 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 K931484. The device is classified under product code BZD. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REPLACEMENT BATTER FOR ABBOTT LABS LIFECARE 4100 S?

REPLACEMENT BATTER FOR ABBOTT LABS LIFECARE 4100 S 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 K931484.

When did REPLACEMENT BATTER FOR ABBOTT LABS LIFECARE 4100 S receive FDA 510(k) clearance?

REPLACEMENT BATTER FOR ABBOTT LABS LIFECARE 4100 S received FDA 510(k) clearance on 1994-02-17, under 510(k) number K931484.

Who is the listed applicant for REPLACEMENT BATTER FOR ABBOTT LABS LIFECARE 4100 S?

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 REPLACEMENT BATTER FOR ABBOTT LABS LIFECARE 4100 S?

The FDA product code for REPLACEMENT BATTER FOR ABBOTT LABS LIFECARE 4100 S is BZD.

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Other records listing Portable Power Systems, Inc. as applicant

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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: BZD)

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.

K261262Altis Full Face MaskRespironics, Inc.K253044RXiBreeze PAP System (RXiBreeze 20C)Resvent Medical Technology Co., Ltd.K253553OrionResmed CorpK254104ResScan EssentialsResmed CorpK251920Sleep Apnea Breathing Therapy Mask:JoyMask 20-B Full Face Mask, JoyMask 21-B Full Face MaskDcstar, Inc.K253166F6S Full Face Mask (F6S); P6S Nasal Pillows Interface (P6S)BMC Medical 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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