# Percutaneous Systems, Inc.

- Location (FDA's records): Mountain View, CA
- FDA decisions: 11 (2004–2011): 11 510(k) clearances
- Names in FDA's records: Percutaneous Systems, Inc. (6); Percutaneous Systems, Incorporated (5)
- Product codes: KNY (5), FFL (3), EZD (2), LQR (1)
- Predicates its devices cite: 2 (1 its own); citations of its devices by later devices: 7 (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
- Van-Tec, Inc.: 1 (https://510kreport.com/company/van-tec)

## Firms that cite its devices most
- Rtc Inc.-Memcath Technologies, LLC: 2 (https://510kreport.com/company/rtc-memcath-technologies)
- Ths International, Inc. D/B/A Accordion Medical: 2 (https://510kreport.com/company/ths-international-d-b-a-accordion-medical)
- Solace Therapeutics: 1 (https://510kreport.com/company/solace-therapeutics)
- Xenolith Medical: 1 (https://510kreport.com/company/xenolith-medical)

## Its most-cited devices
- K052048: Accordion (2005), cited by 3
- K042531: Updated Slip Urology Introducer Sheath (2005), cited by 2
- K082803: Coaxial Accordion Stone Management Device, Model: COAC12005 - COA20015 (2008), cited by 1
- K052298: Cystoglide Introducer Sheath (2006), cited by 1

## Recent decisions
- K102887: Accordion Stone Management Device Model AC281205 and AC3814510 (May 16, 2011)
- K090485: Coaxial Accordion Ercp Device, Models C0AC19001, COAC20005, COAC22003 (Jul 22, 2009)
- K082803: Coaxial Accordion Stone Management Device, Model: COAC12005 - COA20015 (Nov 13, 2008)
- K061766: Expressway Intermittent Catheter (Mar 9, 2007)
- K052298: Cystoglide Introducer Sheath (Dec 12, 2006)
- K052134: Cystoglide Dilating Introducer Sheath (Sep 22, 2005)
- K052048: Accordion (Sep 13, 2005)
- K042531: Updated Slip Urology Introducer Sheath (Feb 1, 2005)

Source page: https://510kreport.com/company/percutaneous-systems