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FDA 510(k)

3M COLOR LASER IMAGER, MODEL 979

K-Number: K923222 · 1992-09-30

Decision Date1992-09-30
Product CodeLMC
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

3M COLOR LASER IMAGER, MODEL 979 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 1992-09-30 under 510(k) number K923222. The device is classified under product code LMC. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 3M COLOR LASER IMAGER, MODEL 979?

3M COLOR LASER IMAGER, MODEL 979 is a medical device that received FDA 510(k) clearance on 1992-09-30. The listed applicant is 3M Medical Products Group. The 510(k) number is K923222.

When did 3M COLOR LASER IMAGER, MODEL 979 receive FDA 510(k) clearance?

3M COLOR LASER IMAGER, MODEL 979 received FDA 510(k) clearance on 1992-09-30, under 510(k) number K923222.

Who is the listed applicant for 3M COLOR LASER IMAGER, MODEL 979?

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 COLOR LASER IMAGER, MODEL 979?

The FDA product code for 3M COLOR LASER IMAGER, MODEL 979 is LMC.

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 Medical Products Group 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.

View all 12 devices →

Related Devices (Code: LMC)

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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