510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K860761Substantially Equivalent

Multi-Image Camera, Series 2100, Model #2100-06

Lenzar Optics Corp., Riviera Beach FL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K860761 is the FDA 510(k) clearance record for MULTI-IMAGE CAMERA, SERIES 2100, MODEL #2100-06, a class II device, cleared for Lenzar Optics Corp. on under FDA product code LMC (Camera, Multi Format, Radiological). FDA records list one 510(k) clearance for Lenzar Optics Corp. As of , FDA records show no recalls naming K860761.

Clearance record

Decision date
Received
(32 days to decision)
Product code
LMC Camera, Multi Format, Radiological
Regulation
21 CFR 892.2040
Device class
Class II
Review panel
Radiology
Applicant
Lenzar Optics Corp. 1006 W. 15th St., Riviera Beach FL
Third party review
No

Clearances, product code LMC

Trailing 12 months

FDA records hold no clearances under product code LMC in the trailing twelve months.

FDA records show no clearances under product code LMC in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code LMC, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260