# Sentry Medical Products, Inc.

- Location (FDA's records): Santa Ana, CA
- FDA decisions: 13 (1983–1996): 13 510(k) clearances
- Product codes: DRX (5), GXY (2), DSA (2), FMT (1), FOS (1), BTX (1), JOS (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
- Target Therapeutics: 1 (https://510kreport.com/company/target-therapeutics)

## Its most-cited devices
- K851522: Diagnostic Ecg Disposable Electrode (1985), cited by 1

## Recent decisions
- K962122: Sentry Radiotranslucent Ecg Electrodes (Jul 24, 1996)
- K955636: Sentry Disposable Dispersive Electrode (Mar 27, 1996)
- K942827: Sentry Insertion Tray (Nov 2, 1994)
- K934000: Sentry Aqueous Gel Ecg Electrodes (Aug 30, 1994)
- K935098: Baby Board (Feb 15, 1994)
- K933603: Leadwire (Jan 18, 1994)
- K932704: Patient Cable (Dec 27, 1993)
- K881670: Accutemp Plus (Nov 22, 1988)

Source page: https://510kreport.com/company/sentry-medical-products