# Survivalink Corp.

- Location (FDA's records): Minnetonka, MN
- FDA decisions: 7 (1995–2002): 7 510(k) clearances
- Product codes: MKJ (6), LDD (1)
- Predicates its devices cite: 7 (3 its own); citations of its devices by later devices: 11 (3 its own)
- Recalls linked to its devices: 4 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Katecho, Inc.: 2 (https://510kreport.com/company/katecho)
- Cardiac Science Corporation: 1 (https://510kreport.com/company/cardiac-science)
- Heartstream, Inc.: 1 (https://510kreport.com/company/heartstream)

## Firms that cite its devices most
- Cardiac Science Corporation: 7 (https://510kreport.com/company/cardiac-science)
- Physio-Control Corp.: 1 (https://510kreport.com/company/physio-control)

## Its most-cited devices
- K011901: Firstsave Star Biphasic, Model 9210/9200 (2002), cited by 3
- K010214: Firstsave Biphasic Model #9200 and 9210 (2001), cited by 2
- K971149: SVL-9130 Defibrillation Electrode (1997), cited by 2
- K982264: Firstsave Biphasic Models 9200 and 9210 (1999), cited by 2
- K970481: V2 (1997), cited by 1
- K940445: Vivalink Aed Defibrillator (1995), cited by 1

## Recent decisions
- K011901: Firstsave Star Biphasic, Model 9210/9200 (Feb 1, 2002)
- K010214: Firstsave Biphasic Model #9200 and 9210 (Feb 22, 2001)
- K993072: Survivalink Multifunctional Electrode (SVL-9630) (Dec 10, 1999)
- K982264: Firstsave Biphasic Models 9200 and 9210 (Jan 25, 1999)
- K970481: V2 (Jul 1, 1997)
- K971149: SVL-9130 Defibrillation Electrode (Jun 23, 1997)
- K940445: Vivalink Aed Defibrillator (Feb 9, 1995)

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