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FDA 510(k)

3M LASER IMAGER

K-Number: K843502 · 1984-11-29

Applicant3M Company
Decision Date1984-11-29
Product CodeLMC
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

3M LASER IMAGER is the device name listed in this FDA 510(k) record. The listed applicant is 3M Company. It received FDA 510(k) clearance on 1984-11-29 under 510(k) number K843502. 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?

3M LASER IMAGER is a medical device that received FDA 510(k) clearance on 1984-11-29. The listed applicant is 3M Company. The 510(k) number is K843502.

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

3M LASER IMAGER received FDA 510(k) clearance on 1984-11-29, under 510(k) number K843502.

Who is the listed applicant for 3M LASER IMAGER?

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 LASER IMAGER?

The FDA product code for 3M LASER IMAGER 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 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: 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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