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FDA 510(k)

MULTI IMAGE CAMERA

K-Number: K828620 · 1982-12-27

ApplicantLenzar Medical Corp.
Decision Date1982-12-27
Product Code
DecisionSubstantially Equivalent

Device Summary

MULTI IMAGE CAMERA is the device name listed in this FDA 510(k) record. The listed applicant is Lenzar Medical Corp.. It received FDA 510(k) clearance on 1982-12-27 under 510(k) number K828620. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTI IMAGE CAMERA?

MULTI IMAGE CAMERA is a medical device that received FDA 510(k) clearance on 1982-12-27. The listed applicant is Lenzar Medical Corp.. The 510(k) number is K828620.

When did MULTI IMAGE CAMERA receive FDA 510(k) clearance?

MULTI IMAGE CAMERA received FDA 510(k) clearance on 1982-12-27, under 510(k) number K828620.

Who is the listed applicant for MULTI IMAGE CAMERA?

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

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.

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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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