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FDA 510(k)

REPLACEMENT RECHARGEABLE BATTERY PACK'S

K-Number: K925449 · 1993-04-29

ApplicantPortable Power Systems, Inc.
Decision Date1993-04-29
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

REPLACEMENT RECHARGEABLE BATTERY PACK'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 1993-04-29 under 510(k) number K925449. The device is classified under product code FRN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REPLACEMENT RECHARGEABLE BATTERY PACK'S?

REPLACEMENT RECHARGEABLE BATTERY PACK'S is a medical device that received FDA 510(k) clearance on 1993-04-29. The listed applicant is Portable Power Systems, Inc.. The 510(k) number is K925449.

When did REPLACEMENT RECHARGEABLE BATTERY PACK'S receive FDA 510(k) clearance?

REPLACEMENT RECHARGEABLE BATTERY PACK'S received FDA 510(k) clearance on 1993-04-29, under 510(k) number K925449.

Who is the listed applicant for REPLACEMENT RECHARGEABLE BATTERY PACK'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 RECHARGEABLE BATTERY PACK'S?

The FDA product code for REPLACEMENT RECHARGEABLE BATTERY PACK'S is FRN.

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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.K934508BATTERY PACK# S1024NCK934439RECHARGEABLE BATTERY PACK FOR CRITIKON 8100 VITAL SIGNS MONITOR

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Related Devices (Code: FRN)

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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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