# K020733: PVS 1500 SDS

- Pathway: 510(k) (Traditional)
- Applicant: Precision Vascular Systems, Inc.
- Decided: Mar 21, 2002 after 15 days
- Product code: KRA (Catheter, Continuous Flush)
- Device class: 2
- Regulation: 21 CFR 870.1210
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K960806 (1996). 2 ancestors in all.
21 later devices descend from it; 3 cite it directly.
0 of 24 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K960806: Turbo Tracker, Target Therapeutics (1996) Summary page 1.
- K001966: Rebar Micro Catheter: Rebar-18 [2.3F], 110 CM, 130 CM, 153 CM, Single Marker Band and 153 CM, Dual Marker Band, Micro Therapeutics, Inc. (2000). Our OCR of the scanned summary read K001968, which is not a number in FDA’s lists. Corrected to the number one digit away whose FDA name carries the summary’s words for the device, “Rebar-18”.

## Most influential descendants
- K032494: PVS 1700 Steerable Delivery System Microcatheter (2003), 20 descendants of its own
- K041123: Rinspiration System,Rinspiration System Short Tip, Models FG01477/FG01703 (2004), 17 descendants of its own
- K050130: Kerberos Proximal Solutions Rispiration System (2005), 16 descendants of its own
- K062275: Rinspiration Catheter System, Models 50135, 550135, P7065, P70135 (2006), 9 descendants of its own
- K080901: Lbi Embolectomy System (2008), 6 descendants of its own

## Indications for use
The PVS 1500 SDS is intended for use in accessing distal peripheral, coronary, and neurovasculature for the sub-selective, controlled, regional delivery of diagnostic, embolic, and therapeutic agents into selected vessels.

Source page: https://510kreport.com/device/K020733
Methodology: https://510kreport.com/methodology