# Seamed Corp.

- Location (FDA's records): Bothell, WA
- FDA decisions: 18 (1982–1992): 18 510(k) clearances
- Product codes: DTE (13), DTC (4), JOQ (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (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
- Biotronik, Inc.: 1 (https://510kreport.com/company/biotronik)

## Its most-cited devices
- K883930: Seamed Model 3300 Dual Chamber Pacing System Analy (1988), cited by 1

## Recent decisions
- K923398: Cpi Model 2215 (Aug 14, 1992)
- K915364: Chronocor VI Model 5012 (Feb 7, 1992)
- K912507: Cpi Model 2215 & Seamed Model 3400 (Sep 3, 1991)
- K910223: Cpi Model 2215/Seamed Model 3400 (Mar 19, 1991)
- K883930: Seamed Model 3300 Dual Chamber Pacing System Analy (Nov 9, 1988)
- K872551: Seamed Model 3200 (Jul 31, 1987)
- K863903: Sea Med Model 6000 (Dec 10, 1986)
- K860462: Seamed Model 3000 (Aug 19, 1986)

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