# Survival Technology, Inc.

- Location (FDA's records): Bethesda, MD
- FDA decisions: 10 (1977–1993): 10 510(k) clearances
- Product codes: DXH (7), FMF (1), DXG (1), DXY (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 3 (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
- Meridian Medical Technologies, Inc.: 1 (https://510kreport.com/company/meridian-medical-technologies)
- Merdian Medical Technologies, Ltd.: 1 (https://510kreport.com/company/merdian-medical-technologies)
- Quality System Consulting: 1 (https://510kreport.com/company/quality-system-consulting)

## Its most-cited devices
- K883614: Cytoguard (R) (1988), cited by 1
- K813101: Cardiobeeper Memory Monitor (1981), cited by 1
- K883843: Cardiobeeper II (1988), cited by 1

## Recent decisions
- K925535: Cardiobeeper (R) CB-Iia (Jan 28, 1993)
- K894799: Cardiobeeper Memory Monitor CB 600 Series (Oct 3, 1989)
- K890461: Cardiobeeper IV (Feb 23, 1989)
- K883843: Cardiobeeper II (Nov 9, 1988)
- K883614: Cytoguard (R) (Sep 15, 1988)
- K880300: Cardiobeeper (R) Iii (May 12, 1988)
- K844966: Cardiobeeper Profile Monitor (Feb 8, 1985)
- K822093: Stat-Scan (Sep 21, 1982)

Source page: https://510kreport.com/company/survival-technology