Cuda Products Co. - FDA 510(k) Cleared Devices
17
Total
17
Cleared
0
Denied
FDA 510(k) Regulatory Record - Cuda Products Co. General & Plastic Surgery ✕
10 devices
Cleared
Dec 16, 1998
LIGHTSOURCE OR ILLUMINATOR MODEL I-100
General & Plastic Surgery
90d
Cleared
Aug 18, 1998
CUDA PRODUCTS CORP. MODEL M300 (M-300) LIGHTSOURCE
General & Plastic Surgery
75d
Cleared
Jul 09, 1998
CERMAX300 LIGHTSOURCE
General & Plastic Surgery
77d
Cleared
Apr 28, 1998
VIDEO CAMERA/LIGHTSOURCE COMBINATION UNIT MODEL VCL-150
General & Plastic Surgery
90d
Cleared
Apr 30, 1996
LIGHTSOURCE OR ILLUMINATOR
General & Plastic Surgery
43d
Cleared
Nov 18, 1993
CUDA PRODUCTS CORP. MODEL MX2-300 LIGHTSOURCE
General & Plastic Surgery
72d
Cleared
Jun 18, 1990
CUDA SURGICAL LIGHT
General & Plastic Surgery
81d
Cleared
Apr 23, 1990
FIBER OPTIC LIGHT GUIDE OR FIBER OPTIC CABLE
General & Plastic Surgery
48d
Cleared
Sep 28, 1989
CO2 LASER BRONCHOSCOPE COUPLER
General & Plastic Surgery
52d
Cleared
Jun 22, 1989
MODEL M2-150/I-150/M2-150T/M3-150/M2-150,300-300
General & Plastic Surgery
49d