# Gastrotech, Inc.

- Location (FDA's records): Independence, OH
- FDA decisions: 5 (1986–1989): 5 510(k) clearances
- Product codes: KNT (2), FED (1), LRO (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K890658: Syringe Injection Gun Delivery Kits (Oct 3, 1989)
- K890629: Esophageal Overtube (May 31, 1989)
- K883351: Percutaneous Endoscopic Gastrostomy Feeding Tube (Aug 23, 1988)
- K883336: Gastrostomy Feeding Tube (Aug 23, 1988)
- K862853: Syringe Injection Gun (Aug 6, 1986)

Source page: https://510kreport.com/company/gastrotech