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FDA 510(k)

SUPERMAX AUTOMATIC X-RAY PROCESSOR

K-Number: K760905 · 1976-11-19

ApplicantGeneral Electric Co.
Decision Date1976-11-19
Product CodeIXW
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SUPERMAX AUTOMATIC X-RAY PROCESSOR is the device name listed in this FDA 510(k) record. The listed applicant is General Electric Co.. It received FDA 510(k) clearance on 1976-11-19 under 510(k) number K760905. The device is classified under product code IXW. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUPERMAX AUTOMATIC X-RAY PROCESSOR?

SUPERMAX AUTOMATIC X-RAY PROCESSOR is a medical device that received FDA 510(k) clearance on 1976-11-19. The listed applicant is General Electric Co.. The 510(k) number is K760905.

When did SUPERMAX AUTOMATIC X-RAY PROCESSOR receive FDA 510(k) clearance?

SUPERMAX AUTOMATIC X-RAY PROCESSOR received FDA 510(k) clearance on 1976-11-19, under 510(k) number K760905.

Who is the listed applicant for SUPERMAX AUTOMATIC X-RAY PROCESSOR?

The FDA 510(k) record lists General Electric Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SUPERMAX AUTOMATIC X-RAY PROCESSOR?

The FDA product code for SUPERMAX AUTOMATIC X-RAY PROCESSOR is IXW.

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Other records listing General Electric Co. as applicant

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K103489GE VEO RECONSTRUCTION OPTIONK082317GE LUNAR FRAX 10-YEAR FRACTURE RISK SOFTWARE OPTIONK081921GE VIVID E9 ULTRASOUNDK073297GE LOGIQ P6K072952GE ECHOPACK072797GE LOGIQ I COMAPACT ULTRASOUND, GE LOGIQ E COMPACT ULTRASOUND, GE VIVID E COMPACT ULTRASOUND

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Related Devices (Code: IXW)

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.

K111167XTENDER FILM PROCESSOR, SPRINT FILM PROCESSOR MODEL XTENDER MODEL SPRINTVelopex International, Inc.K093503INTRAX FILM PROCESSORVelopex International, Inc.K091628OPTIMAX, COMPACT 2, OPTIMAX 2010, ECOMAXProtec GmbH & Co. KGK024342RADIOGRAPHIC FILM PROCESSOR, MODELS XP400 AND XP1000Daito Co., Ltd.K023801FILM PROCESSOR, MODEL LIFE RAY PRO 1000S.A.I.E.P. S.R.L.K023825FILM PROCESSOR, MODEL LIFE RAY PRO 2500S.A.I.E.P. S.R.L.

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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