Cuda Products Co. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cuda Products Co. - FDA 510(k) Cleared Devices
17
Total
17
Cleared
0
Denied
Cuda Products Co. has 17 FDA 510(k) cleared medical devices. Based in Jacksonville, US.
Historical record: 17 cleared submissions from 1988 to 1998. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Cuda Products Co. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cuda Products Co.
17 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 01, 1998
LIGHTSOURCE OR ILLUMINATOR
Obstetrics & Gynecology
75d
Cleared
Apr 30, 1996
LIGHTSOURCE OR ILLUMINATOR
General & Plastic Surgery
43d
Cleared
May 10, 1995
INTRAORAL VIDEO SCOPE AND WINDOW TUBE
Dental
64d
Cleared
Oct 11, 1994
VIDEO OTOSCOPE
Ear, Nose, Throat
70d
Cleared
Jul 13, 1994
ENDOSCOPE
Gastroenterology & Urology
223d
Cleared
Jan 03, 1994
CUDA PRODUCTS CORP. LIGHTSOURCES
Gastroenterology & Urology
178d
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
FIBEROPTIC HEADLIGHT SYSTEM
Dental
51d
Cleared
Jun 22, 1989
MODEL M2-150/I-150/M2-150T/M3-150/M2-150,300-300
General & Plastic Surgery
49d
Cleared
Jan 20, 1988
LASER LAPAROSCOPY SET
Obstetrics & Gynecology
138d