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FDA 510(k)

ALL-PRO 100

K-Number: K911291 · 1991-07-03

ApplicantAll-Pro Imaging Corp.
Decision Date1991-07-03
Product CodeIXW
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ALL-PRO 100 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 1991-07-03 under 510(k) number K911291. 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 ALL-PRO 100?

ALL-PRO 100 is a medical device that received FDA 510(k) clearance on 1991-07-03. The listed applicant is All-Pro Imaging Corp.. The 510(k) number is K911291.

When did ALL-PRO 100 receive FDA 510(k) clearance?

ALL-PRO 100 received FDA 510(k) clearance on 1991-07-03, under 510(k) number K911291.

Who is the listed applicant for ALL-PRO 100?

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 ALL-PRO 100?

The FDA product code for ALL-PRO 100 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 2010K991435AII-PRO 100 PLUS AND ALL-PRO 200

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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