Cuda Products Co.

FDA Regulatory Profile

Cuda Products Co. appears in FDA public data with 0 recalls, 17 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on Dec 16, 1998.

Summary

Total Recalls
0
510(k) Clearances
17
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K983277LIGHTSOURCE OR ILLUMINATOR MODEL I-100Dec 16, 1998
K981962CUDA PRODUCTS CORP. MODEL M300 (M-300) LIGHTSOURCEAug 18, 1998
K981469CERMAX300 LIGHTSOURCEJul 9, 1998
K980350VIDEO CAMERA/LIGHTSOURCE COMBINATION UNIT MODEL VCL-150Apr 28, 1998
K980166LIGHTSOURCE OR ILLUMINATORApr 1, 1998
K961074LIGHTSOURCE OR ILLUMINATORApr 30, 1996
K951019INTRAORAL VIDEO SCOPE AND WINDOW TUBEMay 10, 1995
K943731VIDEO OTOSCOPEOct 11, 1994
K935818ENDOSCOPEJul 13, 1994
K933369CUDA PRODUCTS CORP. LIGHTSOURCESJan 3, 1994
K934337CUDA PRODUCTS CORP. MODEL MX2-300 LIGHTSOURCENov 18, 1993
K901491CUDA SURGICAL LIGHTJun 18, 1990
K901035FIBER OPTIC LIGHT GUIDE OR FIBER OPTIC CABLEApr 23, 1990
K894962CO2 LASER BRONCHOSCOPE COUPLERSep 28, 1989
K893491MODEL M2-150/I-150/M2-150T/M3-150/M2-150,300-300Jun 22, 1989
K893458FIBEROPTIC HEADLIGHT SYSTEMJun 22, 1989
K873598LASER LAPAROSCOPY SETJan 20, 1988