MULTI-IMAGE CAMERA, SERIES 2100, MODEL #2100-06— 510(k) K860761

Name: FDA 510(k) clearance K860761
Creator: U.S. Food and Drug Administration
Published: 1986-04-01

Substantially Equivalent

Lenzar Optics Corp.

FDA 510(k) clearance K860761 for MULTI-IMAGE CAMERA, SERIES 2100, MODEL #2100-06, Substantially Equivalent on 1986-04-01. Applicant: Lenzar Optics Corp.. Device class: 2.

Clearance details

Applicant: Lenzar Optics Corp.
Product code: Code LMC
Device class: Class 2
Regulation: 21 CFR 892.2040
Advisory panel: Radiology
Date received: 1986-02-28
Decision date: 1986-04-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Riviera Beach, FL, US

Download summary PDF View on FDA.gov ↗

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