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FDA 510(k)

KONICA SRX-201 AUTOMATIC X-RA FILM PROCESSOR

K-Number: K950358 · 1995-03-17

ApplicantStorch Amini & Munves PC
Decision Date1995-03-17
Product CodeIXW
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

KONICA SRX-201 AUTOMATIC X-RA FILM PROCESSOR is the device name listed in this FDA 510(k) record. The listed applicant is Storch Amini & Munves PC. It received FDA 510(k) clearance on 1995-03-17 under 510(k) number K950358. 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 KONICA SRX-201 AUTOMATIC X-RA FILM PROCESSOR?

KONICA SRX-201 AUTOMATIC X-RA FILM PROCESSOR is a medical device that received FDA 510(k) clearance on 1995-03-17. The listed applicant is Storch Amini & Munves PC. The 510(k) number is K950358.

When did KONICA SRX-201 AUTOMATIC X-RA FILM PROCESSOR receive FDA 510(k) clearance?

KONICA SRX-201 AUTOMATIC X-RA FILM PROCESSOR received FDA 510(k) clearance on 1995-03-17, under 510(k) number K950358.

Who is the listed applicant for KONICA SRX-201 AUTOMATIC X-RA FILM PROCESSOR?

The FDA 510(k) record lists Storch Amini & Munves PC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KONICA SRX-201 AUTOMATIC X-RA FILM PROCESSOR?

The FDA product code for KONICA SRX-201 AUTOMATIC X-RA FILM PROCESSOR is IXW.

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 Storch Amini & Munves PC 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.

K950359KONICA LASER IMAGER LI-21

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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