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FDA 510(k)

MULTI-IMAGE CAMERA, SERIES 2100, MODEL #2100-06

K-Number: K860761 · 1986-04-01

ApplicantLenzar Optics Corp.
Decision Date1986-04-01
Product CodeLMC
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MULTI-IMAGE CAMERA, SERIES 2100, MODEL #2100-06 is the device name listed in this FDA 510(k) record. The listed applicant is Lenzar Optics Corp.. It received FDA 510(k) clearance on 1986-04-01 under 510(k) number K860761. 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 MULTI-IMAGE CAMERA, SERIES 2100, MODEL #2100-06?

MULTI-IMAGE CAMERA, SERIES 2100, MODEL #2100-06 is a medical device that received FDA 510(k) clearance on 1986-04-01. The listed applicant is Lenzar Optics Corp.. The 510(k) number is K860761.

When did MULTI-IMAGE CAMERA, SERIES 2100, MODEL #2100-06 receive FDA 510(k) clearance?

MULTI-IMAGE CAMERA, SERIES 2100, MODEL #2100-06 received FDA 510(k) clearance on 1986-04-01, under 510(k) number K860761.

Who is the listed applicant for MULTI-IMAGE CAMERA, SERIES 2100, MODEL #2100-06?

The FDA 510(k) record lists Lenzar Optics Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MULTI-IMAGE CAMERA, SERIES 2100, MODEL #2100-06?

The FDA product code for MULTI-IMAGE CAMERA, SERIES 2100, MODEL #2100-06 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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