G.D. Searle and Co.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
56
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K821159IN-LINE OXYGEN MONITORING SYSTEMMay 25, 1982
K811068BYPASS COILMay 27, 1981
K811071VENOUS OXYGEN PROBEMay 5, 1981
K803238INTRAVASCULAR CATHETERApril 23, 1981
K810630SILICONE ELASTOMER COATED LATEX FOLEYMarch 31, 1981
K810131ADMINISTRATION SETFebruary 26, 1981
K802485SEARLE VASCULAR LOOPSFebruary 12, 1981
K801805METRONIDAZOLE DISCSFebruary 10, 1981
K810112SWR DISPOSABLE PREP RAZORFebruary 4, 1981
K802280WHITE KNIGHT DRAPE SEALOctober 10, 1980
K802213WHITE KNIGHT BOVIE CORD/SUCTION TUBEOctober 10, 1980
K801415LATEX FOLEY CATHETER (HYDROMER COATED)August 20, 1980
K801414ERYTHROCATH INTRAVENOUS CATHETER PLA. U.August 13, 1980
K800815ENTERAL & NASOGASTRIC SOL. ADMIN. SETJuly 21, 1980
K800927WHITE KNIGHT DISP. STERILE BACK GOWNMay 20, 1980
K800928WHITE KNIGHT SUPPLEMENTAL DRAPEMay 20, 1980
K800929WHITE KNIGHT SURGICAL PACKMay 20, 1980
K800609CATHETER STYLETApril 10, 1980
K800608STONE DISLODGERApril 8, 1980
K800610URETHRAL SOUNDApril 8, 1980