American Endoscopy, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
19
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K853274AMERICAN DILATATION SYSTEMOctober 17, 1985
K841384PROXIMA 1 PH MONITORJuly 19, 1984
K833491ENDO BITE BLOCKApril 25, 1984
K840818BIOPSY FORCEPSApril 13, 1984
K833859TAMPONADE BALLOON CUFFJanuary 3, 1984
K833492PERCUTANEOUS ENDOSCOPIC GASTROSCOPYNovember 29, 1983
K832458AUTOMATIC ENDOSCOPEOctober 20, 1983
K821818RETRIEVAL BALLOONSSeptember 24, 1982
K821819PIGTAIL STENTSAugust 20, 1982
K822062BALL TIP COAGULATING ELECTRODESAugust 19, 1982
K821817PIGTAIL NASAL CATHETERSAugust 10, 1982
K822061LAVAGING CATHETERSJuly 20, 1982
K821697INJECTION ASPIRATING NEEDLESJune 25, 1982
K820431E.R.C.P. CANNULASApril 9, 1982
K820429SPIRAL STONE AND RETRIEVAL BASKETSApril 8, 1982
K820430DIATHERMIC SNARESApril 8, 1982
K820239RETRIEVAL FORCEPSMarch 26, 1982
K820240PAPILLOTOMESMarch 26, 1982
K820259STERILE CYTOLOGY BRUSHESMarch 5, 1982