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FDA 510(k)

CURIX CAPACITY FILM CENTER

K-Number: K832603 · 1983-09-29

ApplicantAgfa-Gevaert, Inc.
Decision Date1983-09-29
Product CodeIXW
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CURIX CAPACITY FILM CENTER is the device name listed in this FDA 510(k) record. The listed applicant is Agfa-Gevaert, Inc.. It received FDA 510(k) clearance on 1983-09-29 under 510(k) number K832603. 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 CURIX CAPACITY FILM CENTER?

CURIX CAPACITY FILM CENTER is a medical device that received FDA 510(k) clearance on 1983-09-29. The listed applicant is Agfa-Gevaert, Inc.. The 510(k) number is K832603.

When did CURIX CAPACITY FILM CENTER receive FDA 510(k) clearance?

CURIX CAPACITY FILM CENTER received FDA 510(k) clearance on 1983-09-29, under 510(k) number K832603.

Who is the listed applicant for CURIX CAPACITY FILM CENTER?

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

What is the FDA product code for CURIX CAPACITY FILM CENTER?

The FDA product code for CURIX CAPACITY FILM CENTER is IXW.

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Other records listing Agfa-Gevaert, 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.

K882096SCOPIX VIDEO IMAGERK790273MAMMOGRAPHY SYSTEM AND CASSETTE

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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