# Alto Development Corp.

- Location (FDA's records): Farmingdale, NJ
- FDA decisions: 10 (1982–1996): 10 510(k) clearances
- Product codes: GEI (6), DRS (1), GAO (1), FZQ (1), LDF (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: 2 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K964621: A & E Medical Electrocautery Suction Tube with Finger Tip Activator Button (Dec 20, 1996)
- K932513: Labeling for Myo/Wire II Sternotomy Sutures (Jan 7, 1994)
- K931537: A&E Medical Electrosurg Electro W/Non-Stick Coat (Sep 7, 1993)
- K930528: A&E Medical Electrosurgical Connecting Cords (May 17, 1993)
- K914193: A&E Medical Corp Dispos Suct Coag W/Non Stick Coat (Oct 5, 1992)
- K915300: A & EM Medical Electrosurgical Pencil/Accessories (Feb 18, 1992)
- K884783: Raney Clip (Nov 30, 1988)
- K881413: Electro-Cautery Suction Tube (Apr 21, 1988)

Source page: https://510kreport.com/company/alto-development