# K974015: Argyle Quick- Picc Peripherally Inserted Central Catheter- Picc Trays, Argyle Quick- Picc Peripherally Inserted Central

- Pathway: 510(k) (Traditional)
- Applicant: Davis & Geck, Inc.
- Decided: May 18, 1998 after 208 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
No predicates in its family tree.
3 later devices descend from it; 3 cite it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Bard Access System’s Per-Q-Cath PICC: named in the summary without a submission number
- (no number) Luther Medical Company's L-Cath PICC: named in the summary without a submission number

## Most influential descendants
- K061936: Kendall Argyle Neonatal/Pediatric Picc, Model 43311 (2006), 1 descendant of its own
- K042461: Kendall Argyle 2 FR Double Lumen Neonatal/Pediatric Picc, Model 43304 (2004), 1 descendant of its own
- K132567: Argyle Peripherally Inserted Central Catheter Single Lumen, Argyle Peripherally Inserted Central Catheter Dual Lumen (2013), 0 descendants of its own

## Indications for use
The Quick-PICC Catheter System is designed for cases in which venous catheterization or long term 1.V. administration is necessary. Placement is routinely achieved from a peripheral venous site, but the catheter may be placed via subclavian cut-down as well. The Quick-PICC may be used to administer fluids for hydration and parenteral nutrition, as well as other commonly used intravenous medications such as antibiotics, vasopressors, chemotherapy, and analgesics.

Source page: https://510kreport.com/device/K974015
Methodology: https://510kreport.com/methodology