American Cystocope Makers, Inc. - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
FDA 510(k) Regulatory Record - American Cystocope Makers, Inc. Gastroenterology & Urology ✕
6 devices
Cleared
Sep 29, 1983
STERILE FLUID PRODUCING UNIT #EP550
Gastroenterology & Urology
97d
Cleared
Jan 15, 1981
ACMI BIPOLAR HEMOSTATIC ELECTRODE
Gastroenterology & Urology
28d
Cleared
Jul 30, 1979
ACMI RIGI-FLEX NEPHORSCOPE
Gastroenterology & Urology
35d
Cleared
Oct 21, 1976
MODEL TX-8 PANENDOSCOPE
Gastroenterology & Urology
8d
Cleared
Aug 30, 1976
AIR WATER SOURCE (ACMI MODEL 710)
Gastroenterology & Urology
14d
Cleared
Aug 30, 1976
COLONOSCOPE, 2-CHANNEL LOG (ACMI TX-92)
Gastroenterology & Urology
14d