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FDA 510(k)

3M XP-2000 X-RAY FILM PROCESSOR

K-Number: K940558 · 1994-03-22

Applicant3M Company
Decision Date1994-03-22
Product CodeIXW
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

3M XP-2000 X-RAY FILM PROCESSOR is the device name listed in this FDA 510(k) record. The listed applicant is 3M Company. It received FDA 510(k) clearance on 1994-03-22 under 510(k) number K940558. 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 XP-2000 X-RAY FILM PROCESSOR?

3M XP-2000 X-RAY FILM PROCESSOR is a medical device that received FDA 510(k) clearance on 1994-03-22. The listed applicant is 3M Company. The 510(k) number is K940558.

When did 3M XP-2000 X-RAY FILM PROCESSOR receive FDA 510(k) clearance?

3M XP-2000 X-RAY FILM PROCESSOR received FDA 510(k) clearance on 1994-03-22, under 510(k) number K940558.

Who is the listed applicant for 3M XP-2000 X-RAY FILM PROCESSOR?

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

What is the FDA product code for 3M XP-2000 X-RAY FILM PROCESSOR?

The FDA product code for 3M XP-2000 X-RAY FILM PROCESSOR is IXW.

Related Clinical Trials

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.

Other records listing 3M Company 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.

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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.

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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