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.

American Cystocope Makers, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

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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