# Piccolo Medical, Inc.

- Location (FDA's records): San Francisco, CA
- FDA decisions: 4 (2021–2025): 4 510(k) clearances
- Product codes: LJS (4)
- 510(k) review time since 2016: median 202 days, against 171 for FDA's reviews in the same codes and years (1 of 3 faster)
- Predicates its devices cite: 9 (4 its own); citations of its devices by later devices: 4 (4 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
- AngioDynamics, Inc.: 1 (https://510kreport.com/company/angiodynamics)
- Nurse Assist, Inc.: 1 (https://510kreport.com/company/nurse-assist)
- Arrow International, LLC (A subsidiary of Teleflex, Inc.): 1 (https://510kreport.com/company/arrow-international-a-subsidiary-of-teleflex)
- Navi Medical Technologies: 1 (https://510kreport.com/company/navi-medical-technologies)
- C.R. Bard, Inc.: 1 (https://510kreport.com/company/cr-bard)

## Its most-cited devices
- K200037: Piccolo Medical SmartPICC System (2021), cited by 2
- K240486: PM2 System and ECGuide Connector (2024), cited by 2

## Recent decisions
- K252792: PM2™ System with ECGuide™ Connector (Nov 17, 2025)
- K243484: PM2+ System and SmartPICC Stylet (May 29, 2025)
- K240486: PM2 System and ECGuide Connector (Sep 8, 2024)
- K200037: Piccolo Medical SmartPICC System (Jan 22, 2021)

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