American Medical Products, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
30
Inspections
1
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K922290SINGLE-STEP PREGNANCY, HCG TESTJuly 9, 1992
K862221E-Z CLEANSeptember 12, 1986
K861251AMP CLOSED URINARY DRAINAGE BAG, 1011 & 1011NApril 17, 1986
K830881AMPERCIDE DISINFECTANT ACCESSORY TO -June 2, 1983
K823827AMP 80/2 OUTFLOW MONITOR MODIFICATIONMarch 17, 1983
K822545CCPD CYCLER SET W/5 PRONGED CONNECTOROctober 13, 1982
K822550SAFE LOCK TITANIUM ADAPTER SETOctober 13, 1982
K822546SAFE LOCK SEALING CAPSOctober 13, 1982
K822543CAPD SAFE LOCK TRANSFER SETOctober 13, 1982
K822544SAFE LOCK SEALING CAP LOctober 13, 1982
K822551AMP CAPD UNISPIKE AMINISTRATION SETOctober 13, 1982
K822548SAFE LOCK CATHETER S-3October 13, 1982
K822549CCPD CYCLER SET W/5 PRONGED SAFE LOCKOctober 13, 1982
K822547CAPD BELTSeptember 9, 1982
K813069PERITONEAL DIALYSIS CYCLER SETNovember 16, 1981
K811986THE AMP 80/2 PEDIATRIC CYCLER SYSTEMAugust 31, 1981
K811917I.V. ADMIN. SETS FOR THE AMP MARK IV PMPJuly 23, 1981
K811918AMP MARK IV INFUSION PUMPJuly 20, 1981
K810840AMP PERITONEAL DIALYSIS PREP KITApril 29, 1981
K810670CCPD CYCLER SETMarch 24, 1981