510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K821753Substantially Equivalent

A O Fiber Optic Illumination, 1185A

Warner-Lambert Co., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K821753 is the FDA 510(k) clearance record for A O FIBER OPTIC ILLUMINATION, 1185A, a class II device, cleared for Warner-Lambert Co. on under FDA product code FCR (Light Source, Photographic, Fiberoptic). FDA records list 50 510(k) clearances for Warner-Lambert Co., from to . As of , FDA records show no recalls naming K821753.

Clearance record

Decision date
Received
(9 days to decision)
Product code
FCR Light Source, Photographic, Fiberoptic
Regulation
21 CFR 876.1500
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Warner-Lambert Co. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code FCR

Trailing 12 months

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

FDA records show no clearances under product code FCR in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code FCR, 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