Cuda Products Co.

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K983277LIGHTSOURCE OR ILLUMINATOR MODEL I-100December 16, 1998
K981962CUDA PRODUCTS CORP. MODEL M300 (M-300) LIGHTSOURCEAugust 18, 1998
K981469CERMAX300 LIGHTSOURCEJuly 9, 1998
K980350VIDEO CAMERA/LIGHTSOURCE COMBINATION UNIT MODEL VCL-150April 28, 1998
K980166LIGHTSOURCE OR ILLUMINATORApril 1, 1998
K961074LIGHTSOURCE OR ILLUMINATORApril 30, 1996
K951019INTRAORAL VIDEO SCOPE AND WINDOW TUBEMay 10, 1995
K943731VIDEO OTOSCOPEOctober 11, 1994
K935818ENDOSCOPEJuly 13, 1994
K933369CUDA PRODUCTS CORP. LIGHTSOURCESJanuary 3, 1994
K934337CUDA PRODUCTS CORP. MODEL MX2-300 LIGHTSOURCENovember 18, 1993
K901491CUDA SURGICAL LIGHTJune 18, 1990
K901035FIBER OPTIC LIGHT GUIDE OR FIBER OPTIC CABLEApril 23, 1990
K894962CO2 LASER BRONCHOSCOPE COUPLERSeptember 28, 1989
K893491MODEL M2-150/I-150/M2-150T/M3-150/M2-150,300-300June 22, 1989
K893458FIBEROPTIC HEADLIGHT SYSTEMJune 22, 1989
K873598LASER LAPAROSCOPY SETJanuary 20, 1988