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FDA 510(k)

3M LASER IMAGER MODEL 969

K-Number: K923075 · 1992-09-23

Applicant3M Medical Products Group
Decision Date1992-09-23
Product CodeLMC
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

3M LASER IMAGER MODEL 969 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 1992-09-23 under 510(k) number K923075. 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 LASER IMAGER MODEL 969?

3M LASER IMAGER MODEL 969 is a medical device that received FDA 510(k) clearance on 1992-09-23. The listed applicant is 3M Medical Products Group. The 510(k) number is K923075.

When did 3M LASER IMAGER MODEL 969 receive FDA 510(k) clearance?

3M LASER IMAGER MODEL 969 received FDA 510(k) clearance on 1992-09-23, under 510(k) number K923075.

Who is the listed applicant for 3M LASER IMAGER MODEL 969?

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 LASER IMAGER MODEL 969?

The FDA product code for 3M LASER IMAGER MODEL 969 is LMC.

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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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