# American Cystocope Makers, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 9 (1976–1983): 9 510(k) clearances
- Product codes: FAK (1), FGA (1), OCX (1), FEH (1), FOG (1), GEI (1), EOQ (1), FDF (1), LJH (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 2 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Gyrus Acmi, Inc.: 1 (https://510kreport.com/company/gyrus-acmi)
- Acmi Corporation: 1 (https://510kreport.com/company/acmi)

## Its most-cited devices
- K791182: Acmi Rigi-Flex Nephorscope (1979), cited by 1
- K803214: Acmi Bipolar Hemostatic Electrode (1981), cited by 1

## Recent decisions
- K832040: Sterile Fluid Producing Unit #EP550 (Sep 29, 1983)
- K812637: Acmi Bipolar Hemostatic Source (Oct 26, 1981)
- K811218: Acmi Aspirator Kit #8808 (Jul 1, 1981)
- K803214: Acmi Bipolar Hemostatic Electrode (Jan 15, 1981)
- K791182: Acmi Rigi-Flex Nephorscope (Jul 30, 1979)
- K770754: Duodenoscope, Molel TX-6 (Apr 28, 1977)
- K760822: Model TX-8 Panendoscope (Oct 21, 1976)
- K760451: Air Water Source (Acmi Model 710) (Aug 30, 1976)

Source page: https://510kreport.com/company/american-cystocope-makers