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FDA 510(k)

REPLACEMENT BATERY FOR GE AMX-4 PORT. X-RAY MACH.

K-Number: K931483 · 1994-02-17

ApplicantPortable Power Systems, Inc.
Decision Date1994-02-17
Product CodeIZL
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

REPLACEMENT BATERY FOR GE AMX-4 PORT. X-RAY MACH. 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 K931483. The device is classified under product code IZL. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REPLACEMENT BATERY FOR GE AMX-4 PORT. X-RAY MACH.?

REPLACEMENT BATERY FOR GE AMX-4 PORT. X-RAY MACH. 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 K931483.

When did REPLACEMENT BATERY FOR GE AMX-4 PORT. X-RAY MACH. receive FDA 510(k) clearance?

REPLACEMENT BATERY FOR GE AMX-4 PORT. X-RAY MACH. received FDA 510(k) clearance on 1994-02-17, under 510(k) number K931483.

Who is the listed applicant for REPLACEMENT BATERY FOR GE AMX-4 PORT. X-RAY MACH.?

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 BATERY FOR GE AMX-4 PORT. X-RAY MACH.?

The FDA product code for REPLACEMENT BATERY FOR GE AMX-4 PORT. X-RAY MACH. is IZL.

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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 #PMX120-18AK933065BATTERY PACK# S1009LAK934439RECHARGEABLE BATTERY PACK FOR CRITIKON 8100 VITAL SIGNS MONITORK934508BATTERY PACK# S1024NC

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Related Devices (Code: IZL)

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.

K260236XLITEGEMSS HEALTHCARE CO., LTD.K253058Portable DR Imaging SystemShantou Institute of Ultrasonic Instruments Co., Ltd.K260085RAYMO Mobile X-ray System (Model: RAYMO)DRGEM CorporationK253185Lux HD Detectors, DRX-LC Detector, DRX-Revolution Mobile X-Ray SystemCarestream HealthK253244AirRay-mini 80A, AirRay-mini 90A, AirRay-mini 80F, AirRay-mini 90F (AirRay-mini)Poskom Co., Ltd.K250976Airbile-100Poskom 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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