# Memtec Corp.

- Location (FDA's records): Salem, NH
- FDA decisions: 4 (1997–2019): 4 510(k) clearances
- Names in FDA's records: Memtec Corp. (3); Memtec Corporation (1)
- Product codes: MWJ (1), DSI (1), DSH (1), DPS (1)
- Predicates its devices cite: 11 (1 its own); citations of its devices by later devices: 3 (1 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Datrix: 2 (https://510kreport.com/company/datrix)
- Qrs Diagnostic, LLC: 2 (https://510kreport.com/company/qrs-diagnostic)
- Rozinn Electronics, Inc.: 1 (https://510kreport.com/company/rozinn-electronics)
- North East Monitoring, Inc.: 1 (https://510kreport.com/company/north-east-monitoring)
- Ela Medical, Inc.: 1 (https://510kreport.com/company/ela-medical)
- Braemar, Inc.: 1 (https://510kreport.com/company/braemar)
- Preventice: 1 (https://510kreport.com/company/preventice)
- Micromedical, Inc.: 1 (https://510kreport.com/company/micromedical)

## Firms that cite its devices most
- Telemed Solutions, Inc.: 1 (https://510kreport.com/company/telemed-solutions)
- Applied Cardiac Systems: 1 (https://510kreport.com/company/applied-cardiac-systems)

## Its most-cited devices
- K102723: Model 950-12L Holter Recorder Without Analysis (2010), cited by 2
- K103427: Mobileecg System (2011), cited by 1

## Recent decisions
- K181658: MobileECG 2 BT (Mar 26, 2019)
- K103427: Mobileecg System (Mar 24, 2011)
- K102723: Model 950-12L Holter Recorder Without Analysis (Dec 9, 2010)
- K944180: MODEL 700 (Mar 7, 1997)

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