# K092629: SNM Firmgrip

- Pathway: 510(k) (Special)
- Applicant: Flexicath, Ltd.
- Decided: Sep 25, 2009 after 29 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: 5 generations back to K930473 (1994). 8 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 10 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K080793: Firmgrip, Flexicath, Ltd. (2008) Summary page 2.

## Most influential descendants
- K111939: M/29TM - Pressure Injectable (2012), 0 descendants of its own

## Indications for use
The SNM FirmGripTM - Peripherally Inserted Catheter Device is intended for use in patients requiring repeated access to the peripheral venous system for infusion or injection intravenous therapies and/or blood sampling.

Source page: https://510kreport.com/device/K092629
Methodology: https://510kreport.com/methodology