Cuda Products Co.

Jacksonville, FL, US

Cuda Products Co. appears in FDA device records in Jacksonville, FL. FDA records list 17 510(k) clearances between 1988-01-20 and 1998-12-16, no PMA records and no registered establishments. As of 2026-09-10, FDA records show no recalls for this company.

510(k) clearances: 17
PMA records: 0
Recall records: 0
Registered establishments: 0

510(k) clearance history

FDA records hold 17 510(k) clearances for Cuda Products Co. between 1988 and 1998. The busiest year on record is 1998, with 5. The most recent is 1998, with 5.

Clearances by year, as a table

510(k) clearance decisions for Cuda Products Co., by decision year
Year	Clearances
1988	1
1989	3
1990	2
1993	1
1994	3
1995	1
1996	1
1998	5

510(k) clearances on record, most recent first
K number	Device	Product code	Decision	Decision date
K983277	LIGHTSOURCE OR ILLUMINATOR MODEL I-100	HBI	Substantially Equivalent	1998-12-16
K981962	CUDA PRODUCTS CORP. MODEL M300 (M-300) LIGHTSOURCE	FSS	Substantially Equivalent	1998-08-18
K981469	CERMAX300 LIGHTSOURCE	FSS	Substantially Equivalent	1998-07-09
K980350	VIDEO CAMERA/LIGHTSOURCE COMBINATION UNIT MODEL VCL-150	GCJ	Substantially Equivalent	1998-04-28
K980166	LIGHTSOURCE OR ILLUMINATOR	HET	Substantially Equivalent	1998-04-01
K961074	LIGHTSOURCE OR ILLUMINATOR	FSS	Substantially Equivalent	1996-04-30
K951019	INTRAORAL VIDEO SCOPE AND WINDOW TUBE	EIA	Substantially Equivalent	1995-05-10
K943731	VIDEO OTOSCOPE	ERA	Substantially Equivalent	1994-10-11
K935818	ENDOSCOPE	GDB	Substantially Equivalent	1994-07-13
K933369	CUDA PRODUCTS CORP. LIGHTSOURCES	FCW	Substantially Equivalent	1994-01-03
K934337	CUDA PRODUCTS CORP. MODEL MX2-300 LIGHTSOURCE	FSW	Substantially Equivalent	1993-11-18
K901491	CUDA SURGICAL LIGHT	FST	Substantially Equivalent	1990-06-18
K901035	FIBER OPTIC LIGHT GUIDE OR FIBER OPTIC CABLE	FST	Substantially Equivalent	1990-04-23
K894962	CO2 LASER BRONCHOSCOPE COUPLER	GEX	Substantially Equivalent	1989-09-28
K893491	MODEL M2-150/I-150/M2-150T/M3-150/M2-150,300-300	FST	Substantially Equivalent	1989-06-22
K893458	FIBEROPTIC HEADLIGHT SYSTEM	EBA	Substantially Equivalent	1989-06-22
K873598	LASER LAPAROSCOPY SET	HET	Substantially Equivalent	1988-01-20

Registered establishments

No FDA establishment registrations recorded against this company.

FDA product codes

Recall records

No recall records for this company in the ingested FDA data.

Verification record

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Data as of 2026-09-28, FDA export datePage updated 2026-09-05Source: openFDA, public domain