Medical Device Manufacturer · US , Mchenry , IL

American Cystocope Makers, Inc. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1976

Total

Cleared

Denied

American Cystocope Makers, Inc. has 9 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 9 cleared submissions from 1976 to 1983. Primary specialty: Gastroenterology & Urology.

Browse the FDA 510(k) cleared devices submitted by American Cystocope Makers, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - American Cystocope Makers, Inc.

9 devices

1-9 of 9

Cleared Sep 29, 1983

STERILE FLUID PRODUCING UNIT #EP550

K832040 · LJH

Gastroenterology & Urology · 97d

Cleared Oct 26, 1981

ACMI BIPOLAR HEMOSTATIC SOURCE

K812637 · GEI

General & Plastic Surgery · 41d

Cleared Jul 01, 1981

ACMI ASPIRATOR KIT #8808

K811218 · EOQ

Ear, Nose, Throat · 58d

Cleared Jan 15, 1981

ACMI BIPOLAR HEMOSTATIC ELECTRODE

K803214 · FEH

Gastroenterology & Urology · 28d

Cleared Jul 30, 1979

ACMI RIGI-FLEX NEPHORSCOPE

K791182 · FGA

Gastroenterology & Urology · 35d

Cleared Apr 28, 1977

DUODENOSCOPE, MOLEL TX-6

K770754 · FOG

Anesthesiology · 3d

Cleared Oct 21, 1976

MODEL TX-8 PANENDOSCOPE

K760822 · FAK

Gastroenterology & Urology · 8d

Cleared Aug 30, 1976

AIR WATER SOURCE (ACMI MODEL 710)

K760451 · OCX

Gastroenterology & Urology · 14d

Cleared Aug 30, 1976

COLONOSCOPE, 2-CHANNEL LOG (ACMI TX-92)

K760452 · FDF

Gastroenterology & Urology · 14d

American Cystocope Makers, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - American Cystocope Makers, Inc.

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