# American Heyer Schulte

- Location (FDA's records): Mchenry, IL
- FDA decisions: 13 (1980–1984): 13 510(k) clearances
- Product codes: JXG (4), GCY (2), GDW (2), LCJ (1), FTL (1), LKG (1), IWJ (1), JCY (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 4 (0 its own)
- Recalls linked to its devices: 5 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Inmed Corp.: 1 (https://510kreport.com/company/inmed)
- Integra LifeSciences Corporation: 1 (https://510kreport.com/company/integra-lifesciences)
- Specialty Surgical Products, Inc.: 1 (https://510kreport.com/company/specialty-surgical-products)
- Neurocare Group: 1 (https://510kreport.com/company/neurocare-group)

## Its most-cited devices
- K801766: Jackson-Pratt Large Vol. Closed Wound (1980), cited by 1
- K820247: External Ventricular Drainage Sys. (1982), cited by 1
- K802586: American Heyer-Schulte Low Profile Valve (1980), cited by 1
- K811288: Spetzler Lumbar-Peritoneal System (1981), cited by 1

## Recent decisions
- K840172: Ventral Wall Defect Reduct Silo (Jun 27, 1984)
- K834593: One-Piece Shunt (Apr 3, 1984)
- K833502: Radovan Subcutaneous Tissue Expander (Feb 3, 1984)
- K833698: Amer. V. Mueller Surg. Staples Ila (Jan 25, 1984)
- K833704: Amer. V. Mueller Surgicalstaples-Cartr (Dec 29, 1983)
- K832738: Heyer-Schulte Afterloading Catheter (Sep 29, 1983)
- K823790: Ventricular Access System (Apr 28, 1983)
- K822096: Chemotherapy Infusion Catheter (Apr 12, 1983)

Source page: https://510kreport.com/company/american-heyer-schulte