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FDA 510(k)

BATTERY PACK# S1009LA

K-Number: K933065 · 1994-02-17

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

Device Summary

BATTERY PACK# S1009LA 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 K933065. The device is classified under product code DPS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BATTERY PACK# S1009LA?

BATTERY PACK# S1009LA 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 K933065.

When did BATTERY PACK# S1009LA receive FDA 510(k) clearance?

BATTERY PACK# S1009LA received FDA 510(k) clearance on 1994-02-17, under 510(k) number K933065.

Who is the listed applicant for BATTERY PACK# S1009LA?

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# S1009LA?

The FDA product code for BATTERY PACK# S1009LA is DPS.

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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: DPS)

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.

K254255S-Patch CardioAIWellysis Corp.K252463SE-1202 Series Electrocardiograph (Model: SE-1202, SE-1202E)Edan Instruments, Inc.K251670MAC 7 Resting ECG Analysis SystemGe Medical Systems Information Technologies, Inc.K252361AccurECG Analysis System (v2.0)Accurkardia, Inc.K252474Withings BeamO (SCT02)WithingsK250569Cardiologs Holter PlatformPhilips France Commercial

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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