Britt Corp., Inc.

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K003828VASO PRESS DVT FOOT GARMENT #VP 520May 18, 2001
K991038VASO PRESS DVT SYSTEM, MODELS VP500, VP501June 22, 2000
K974393VASO PRESS SYSTEMMarch 19, 1999
K860977MODEL 545-45 FOR NEUROLOGICAL SURGICAL APPLICATIONOctober 16, 1986
K860975MODEL 545-45 LASER FOR EAR, NOSE & THROATJuly 18, 1986
K860974MODEL 545-45 LASER FOR DERMA., POD., SURGICALJuly 7, 1986
K860277MODEL 525-25 WATT C02 LASER FOR EAR, NOSE & THROATMay 6, 1986
K860273MODEL 525 - 25 WATT CO2 MEDICAL LASER/PODIATRYApril 23, 1986
K860278MODEL 525-25 WATT CO2 LASER FOR DERMA/PLASTICApril 15, 1986
K851425MODEL J25-25 WATT CO2 LASERNovember 12, 1985
K840020FITNESS LOGGEROctober 26, 1984
K840036FITEXOctober 26, 1984
K833533LASER PHOTOCOAGULATOR 1520-A & KJanuary 30, 1984
K837200BRITT SURGICAL PHOTOCOAGULATOR SYSTEMApril 4, 1983
K837151BLUE GREEN FILTER SYSTEM TO MODEL 152 AND 150 LASER SYSTEMMarch 22, 1983
K813492BRITT KRYPTON LASERS 150K & 152KJanuary 22, 1982
K790694BRITT LENS COMPUTERAugust 10, 1979