510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K933369Substantially Equivalent

Cuda Products Corp. Lightsources

Cuda Products Co., Jacksonville FL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K933369 is the FDA 510(k) clearance record for CUDA PRODUCTS CORP. LIGHTSOURCES, a class II device, cleared for Cuda Products Co. on under FDA product code FCW (Light Source, Fiberoptic, Routine). FDA records list 17 510(k) clearances for Cuda Products Co., from to . As of , FDA records show no recalls naming K933369.

Clearance record

Decision date
Received
(178 days to decision)
Product code
FCW Light Source, Fiberoptic, Routine
Regulation
21 CFR 876.1500
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Cuda Products Co. 6000 Powers Ave., Jacksonville FL
510(k) summary
Statement
Third party review
No

Clearances, product code FCW

Trailing 12 months

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

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