# Upstream Peripheral Technologies

- Location (FDA's records): Philedelphia, PA
- FDA decisions: 5 (2012–2022): 5 510(k) clearances
- Names in FDA's records: Upstream Peripheral Technologies (3); Upstream Peripheral Technologies, Ltd. (2)
- Product codes: DQY (3), PDU (1), DYB (1)
- Predicates its devices cite: 7 (1 its own); citations of its devices by later devices: 1 (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
- Spectranetics Corp.: 2 (https://510kreport.com/company/spectranetics)
- Endocross, Ltd.: 1 (https://510kreport.com/company/endocross)
- Lumend, Inc.: 1 (https://510kreport.com/company/lumend)
- Asahi Intecc Co., Ltd.: 1 (https://510kreport.com/company/asahi-intecc)
- Becton Dickinson Infusion Therapy Systems, Inc.: 1 (https://510kreport.com/company/becton-dickinson-infusion-therapy-systems)

## Its most-cited devices
- K182937: Upstream GoBack Crossing Catheter (2019), cited by 1

## Recent decisions
- K211802: GoBack Crossing Catheter (Mar 1, 2022)
- K182937: Upstream GoBack Crossing Catheter (May 23, 2019)
- K120964: Upstream GR Catheter (May 25, 2012)
- K112887: Upstream Needle Holder, Upstream Needle Holder with Shut-Off Connector (Mar 21, 2012)
- K112886: Upstream Support Catheter (Feb 23, 2012)

Source page: https://510kreport.com/company/upstream-peripheral-technologies