American Cystocope Makers, Inc.
American Cystocope Makers, Inc. holds FDA 510(k) medical device clearances, first cleared 1976, most recent 1983.
Top product codes for American Cystocope Makers, Inc.
Recent clearances by American Cystocope Makers, Inc.
- K832040 — STERILE FLUID PRODUCING UNIT #EP550
- K812637 — ACMI BIPOLAR HEMOSTATIC SOURCE
- K811218 — ACMI ASPIRATOR KIT #8808
- K803214 — ACMI BIPOLAR HEMOSTATIC ELECTRODE
- K791182 — ACMI RIGI-FLEX NEPHORSCOPE
- K770754 — DUODENOSCOPE, MOLEL TX-6
- K760822 — MODEL TX-8 PANENDOSCOPE
- K760451 — AIR WATER SOURCE (ACMI MODEL 710)
- K760452 — COLONOSCOPE, 2-CHANNEL LOG (ACMI TX-92)
Data sourced from openFDA. This site is unofficial and independent of the FDA.