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FDA 510(k)

3M LASER IMAGER XL

K-Number: K910092 · 1991-04-08

Applicant3M Medical Products Group
Decision Date1991-04-08
Product CodeLMC
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

3M LASER IMAGER XL 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 1991-04-08 under 510(k) number K910092. 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 XL?

3M LASER IMAGER XL is a medical device that received FDA 510(k) clearance on 1991-04-08. The listed applicant is 3M Medical Products Group. The 510(k) number is K910092.

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

3M LASER IMAGER XL received FDA 510(k) clearance on 1991-04-08, under 510(k) number K910092.

Who is the listed applicant for 3M LASER IMAGER XL?

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 XL?

The FDA product code for 3M LASER IMAGER XL 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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