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FDA 510(k)

AII-PRO 100 PLUS AND ALL-PRO 200

K-Number: K991435 · 1999-05-20

ApplicantAll-Pro Imaging Corp.
Decision Date1999-05-20
Product CodeIXW
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

AII-PRO 100 PLUS AND ALL-PRO 200 is the device name listed in this FDA 510(k) record. The listed applicant is All-Pro Imaging Corp.. It received FDA 510(k) clearance on 1999-05-20 under 510(k) number K991435. 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 AII-PRO 100 PLUS AND ALL-PRO 200?

AII-PRO 100 PLUS AND ALL-PRO 200 is a medical device that received FDA 510(k) clearance on 1999-05-20. The listed applicant is All-Pro Imaging Corp.. The 510(k) number is K991435.

When did AII-PRO 100 PLUS AND ALL-PRO 200 receive FDA 510(k) clearance?

AII-PRO 100 PLUS AND ALL-PRO 200 received FDA 510(k) clearance on 1999-05-20, under 510(k) number K991435.

Who is the listed applicant for AII-PRO 100 PLUS AND ALL-PRO 200?

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

What is the FDA product code for AII-PRO 100 PLUS AND ALL-PRO 200?

The FDA product code for AII-PRO 100 PLUS AND ALL-PRO 200 is IXW.

Other records listing All-Pro 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.

K001314MEDSCOPEK001321ALL-PRO 2010K911291ALL-PRO 100

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.K023825FILM PROCESSOR, MODEL LIFE RAY PRO 2500S.A.I.E.P. S.R.L.K023801FILM PROCESSOR, MODEL LIFE RAY PRO 1000S.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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