# K992198: Urethane Picc Line Model Upics-

- Pathway: 510(k) (Special)
- Applicant: Cook, Inc.
- Decided: Aug 27, 1999 after 58 days
- Product code: FOZ (Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days)
- Device class: 2
- Regulation: 21 CFR 880.5200
- 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 K862056 (1986). 1 ancestor in all.
136 later devices descend from it; 2 cite it directly.
16 of 138 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K862056: [Central Venous][Multi-Lumen] Catheter W/Flex Tip, Arrow Intl., Inc. (1986) Summary page 2.
- (no number) Silicone PICC Lines (COOK® Inc.): named in the summary without a submission number
- (no number) Vaxcel™ PICC Lines (Boston Scientific/Medi-Tech®): named in the summary without a submission number

## Most influential descendants
- K021557: Spectrum Silicone Catheter (2003), 126 descendants of its own
- K051991: Powerpicc, Poly Per-Q-Cath, 6 FR TL Poly Per-Q-Cath, Power Hohn and Power Line (2005), 119 descendants of its own
- K070996: 4 FR Single Lumen (SL) Powerpicc Catheter (2007), 66 descendants of its own
- K061179: Powerhickman Long-Term Intravascular Catheter (2006), 47 descendants of its own
- K091953: Pro-Picc (2009), 29 descendants of its own

## Indications for use
Used for venous pressure monitoring, blood sampling and administration of drugs and fluids.

Source page: https://510kreport.com/device/K992198
Methodology: https://510kreport.com/methodology