American Medical Products, Inc. is one of 13877 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
American Medical Products, Inc. - FDA 510(k) Cleared Devices
Recent clearances: SINGLE-STEP PREGNANCY, HCG TEST, E-Z CLEAN, AMP CLOSED URINARY DRAINAGE BAG, 1011 & 1011N
30
Total
30
Cleared
0
Denied
American Medical Products, Inc. has 30 FDA 510(k) cleared gastroenterology & urology devices. Based in Mchenry, US.
Historical record: 30 cleared submissions from 1978 to 1992.
Browse the complete list of FDA 510(k) cleared gastroenterology & urology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - American Medical Products, Inc.
30 devices
Cleared
Jul 09, 1992
SINGLE-STEP PREGNANCY, HCG TEST
Chemistry
55d
Cleared
Sep 12, 1986
E-Z CLEAN
General & Plastic Surgery
93d
Cleared
Apr 17, 1986
AMP CLOSED URINARY DRAINAGE BAG, 1011 & 1011N
Gastroenterology & Urology
15d
Cleared
Jun 02, 1983
AMPERCIDE DISINFECTANT ACCESSORY TO -
Gastroenterology & Urology
76d
Cleared
Mar 17, 1983
AMP 80/2 OUTFLOW MONITOR MODIFICATION
Gastroenterology & Urology
87d
Cleared
Oct 13, 1982
CAPD SAFE LOCK TRANSFER SET
Gastroenterology & Urology
51d
Cleared
Oct 13, 1982
SAFE LOCK SEALING CAP L
Gastroenterology & Urology
51d
Cleared
Oct 13, 1982
CCPD CYCLER SET W/5 PRONGED CONNECTOR
Gastroenterology & Urology
51d
Cleared
Oct 13, 1982
SAFE LOCK SEALING CAPS
Gastroenterology & Urology
50d
Cleared
Oct 13, 1982
SAFE LOCK CATHETER S-3
Gastroenterology & Urology
50d
Cleared
Oct 13, 1982
CCPD CYCLER SET W/5 PRONGED SAFE LOCK
Gastroenterology & Urology
50d
Cleared
Oct 13, 1982
SAFE LOCK TITANIUM ADAPTER SET
Gastroenterology & Urology
50d