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FDA 510(k)

GENERAL ELECTRIC AMX 3

K-Number: K902610 · 1990-07-02

ApplicantPro-Tronics, Inc.
Decision Date1990-07-02
Product CodeIZL
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

GENERAL ELECTRIC AMX 3 is the device name listed in this FDA 510(k) record. The listed applicant is Pro-Tronics, Inc.. It received FDA 510(k) clearance on 1990-07-02 under 510(k) number K902610. 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 GENERAL ELECTRIC AMX 3?

GENERAL ELECTRIC AMX 3 is a medical device that received FDA 510(k) clearance on 1990-07-02. The listed applicant is Pro-Tronics, Inc.. The 510(k) number is K902610.

When did GENERAL ELECTRIC AMX 3 receive FDA 510(k) clearance?

GENERAL ELECTRIC AMX 3 received FDA 510(k) clearance on 1990-07-02, under 510(k) number K902610.

Who is the listed applicant for GENERAL ELECTRIC AMX 3?

The FDA 510(k) record lists Pro-Tronics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GENERAL ELECTRIC AMX 3?

The FDA product code for GENERAL ELECTRIC AMX 3 is IZL.

Related Clinical Trials

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.

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Other records listing Pro-Tronics, 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.

K950971MOBIL C-ARM, REGURBISHED, VARIOUS MODELSK944442GENERAL ELECTRIC AMX 110, AMX II AND AMX 3K891143GENERAL ELECTRIC AMX 110K891142GENERAL ELECTRIC AMX II

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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