# Pulse Biomedical, Inc.

- Location (FDA's records): Norristown, PA
- FDA decisions: 3 (1998–2010): 3 510(k) clearances
- Product codes: DPS (1), LOS (1), DQK (1)
- Predicates its devices cite: 9 (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
- Norav Medical, Ltd.: 1 (https://510kreport.com/company/norav-medical)
- Pinmed, Inc.: 1 (https://510kreport.com/company/pinmed)
- Corscience GmbH & Co. KG: 1 (https://510kreport.com/company/corscience)
- North East Monitoring, Inc.: 1 (https://510kreport.com/company/north-east-monitoring)
- Caird Technology: 1 (https://510kreport.com/company/caird-technology)
- Advanced Medical Products, Inc.: 1 (https://510kreport.com/company/advanced-medical-products)
- Oxford Instruments, Plc.: 1 (https://510kreport.com/company/oxford-instruments)
- Biomedical Systems Corp.: 1 (https://510kreport.com/company/biomedical-systems)

## Firms that cite its devices most
- Ross Medical Technology, Inc.: 2 (https://510kreport.com/company/ross-medical-technology)

## Its most-cited devices
- K100813: QRS Card S-T Segment Analysis Patient Monitoring System Model: QRS Card Usb (2010), cited by 1
- K972255: Pulse Biomedical Inc, QRS Card S-T Segment Analysis Monitoring System (1998), cited by 1
- K042799: QRS-Card Cardiology Suite (2004), cited by 1

## Recent decisions
- K100813: QRS Card S-T Segment Analysis Patient Monitoring System Model: QRS Card Usb (Jul 23, 2010)
- K042799: QRS-Card Cardiology Suite (Oct 22, 2004)
- K972255: Pulse Biomedical Inc, QRS Card S-T Segment Analysis Monitoring System (Jul 7, 1998)

Source page: https://510kreport.com/company/pulse-biomedical