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FDA 510(k)

3M DIGITAL RECORDING AUTOMATIC FILM HANDLING UNIT

K-Number: K912225 · 1991-07-22

Applicant3M Medical Products Group
Decision Date1991-07-22
Product CodeIXW
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

3M DIGITAL RECORDING AUTOMATIC FILM HANDLING UNIT is the device name listed in this FDA 510(k) record. The listed applicant is 3M Medical Products Group. It received FDA 510(k) clearance on 1991-07-22 under 510(k) number K912225. 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 3M DIGITAL RECORDING AUTOMATIC FILM HANDLING UNIT?

3M DIGITAL RECORDING AUTOMATIC FILM HANDLING UNIT is a medical device that received FDA 510(k) clearance on 1991-07-22. The listed applicant is 3M Medical Products Group. The 510(k) number is K912225.

When did 3M DIGITAL RECORDING AUTOMATIC FILM HANDLING UNIT receive FDA 510(k) clearance?

3M DIGITAL RECORDING AUTOMATIC FILM HANDLING UNIT received FDA 510(k) clearance on 1991-07-22, under 510(k) number K912225.

Who is the listed applicant for 3M DIGITAL RECORDING AUTOMATIC FILM HANDLING UNIT?

The FDA 510(k) record lists 3M Medical Products Group as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 3M DIGITAL RECORDING AUTOMATIC FILM HANDLING UNIT?

The FDA product code for 3M DIGITAL RECORDING AUTOMATIC FILM HANDLING UNIT is IXW.

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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.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

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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