Medical Device Manufacturer · US , Jacksonville , FL

Cuda Products Co. - FDA 510(k) Cleared Devices

17 submissions · 17 cleared · Since 1988

Total

Cleared

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.

Cuda Products Co. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Cuda Products Co.

17 devices

1-12 of 17

Cleared Dec 16, 1998

LIGHTSOURCE OR ILLUMINATOR MODEL I-100

K983277 · HBI

General & Plastic Surgery · 90d

Cleared Aug 18, 1998

CUDA PRODUCTS CORP. MODEL M300 (M-300) LIGHTSOURCE

K981962 · FSS

General & Plastic Surgery · 75d

Cleared Jul 09, 1998

CERMAX300 LIGHTSOURCE

K981469 · FSS

General & Plastic Surgery · 77d

Cleared Apr 28, 1998

VIDEO CAMERA/LIGHTSOURCE COMBINATION UNIT MODEL VCL-150

K980350 · GCJ

General & Plastic Surgery · 90d

Cleared Apr 01, 1998

LIGHTSOURCE OR ILLUMINATOR

K980166 · HET

Obstetrics & Gynecology · 75d

Cleared Apr 30, 1996

LIGHTSOURCE OR ILLUMINATOR

K961074 · FSS

General & Plastic Surgery · 43d

Cleared May 10, 1995

INTRAORAL VIDEO SCOPE AND WINDOW TUBE

Ear, Nose, Throat · 70d

Cleared Jul 13, 1994

ENDOSCOPE

K935818 · GDB

Gastroenterology & Urology · 223d

Cleared Jan 03, 1994

CUDA PRODUCTS CORP. LIGHTSOURCES

K933369 · FCW

Gastroenterology & Urology · 178d

Cleared Nov 18, 1993

CUDA PRODUCTS CORP. MODEL MX2-300 LIGHTSOURCE

K934337 · FSW

General & Plastic Surgery · 72d

Cleared Jun 18, 1990

CUDA SURGICAL LIGHT

K901491 · FST

General & Plastic Surgery · 81d

Cuda Products Co. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Cuda Products Co.

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