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FDA 510(k)

AFP 17 X 4 AUTOMATIC FILM PROCESSOR

K-Number: K925885 · 1993-06-09

ApplicantAfp Imaging Corp.
Decision Date1993-06-09
Product CodeIXW
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

AFP 17 X 4 AUTOMATIC FILM PROCESSOR is the device name listed in this FDA 510(k) record. The listed applicant is Afp Imaging Corp.. It received FDA 510(k) clearance on 1993-06-09 under 510(k) number K925885. 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 AFP 17 X 4 AUTOMATIC FILM PROCESSOR?

AFP 17 X 4 AUTOMATIC FILM PROCESSOR is a medical device that received FDA 510(k) clearance on 1993-06-09. The listed applicant is Afp Imaging Corp.. The 510(k) number is K925885.

When did AFP 17 X 4 AUTOMATIC FILM PROCESSOR receive FDA 510(k) clearance?

AFP 17 X 4 AUTOMATIC FILM PROCESSOR received FDA 510(k) clearance on 1993-06-09, under 510(k) number K925885.

Who is the listed applicant for AFP 17 X 4 AUTOMATIC FILM PROCESSOR?

The FDA 510(k) record lists Afp Imaging Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AFP 17 X 4 AUTOMATIC FILM PROCESSOR?

The FDA product code for AFP 17 X 4 AUTOMATIC FILM PROCESSOR is IXW.

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Other records listing Afp Imaging Corp. 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.

K123419EVA SELECT DIGITAL DENTAL IMAGING SYSTEMK072357NEWTOM VG COMPUTED TOMOGRAPHY X-RAY SYSTEMK041120EV APAN DIGITAL, MODEL K1VSM2000K030647EVA DIGITAL DENTAL X-RAY SYSTEMK014144EXTORAL/TESCERA GLAZING RESIN, MODEL T-1804K013176MODIFICATION TO: SENS-A-RAY SYSTEM WITH PROIMAGE SOFTWARE

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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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