# K951683: A-V Impulse System Model 6060

- Pathway: 510(k) (Traditional)
- Applicant: Novamedix, Ltd.
- Decided: Oct 26, 1995 after 198 days
- Product code: JOW (Sleeve, Limb, Compressible)
- Device class: 2
- Regulation: 21 CFR 870.5800
- Recalls of this device: 2 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
21 later devices descend from it; 2 cite it directly.
0 of 22 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K072666: Bioarterial Plus, Arterial Blood Flow Enhancement System (2007), 18 descendants of its own
- K131327: Bioarterial Plus Arterial Blood Flow Enhancement System (2013), 14 descendants of its own
- K181149: Therm-X Pro, Therm-X AT, Therm-X Pro Athlete (2018), 12 descendants of its own
- K190854: Therm-X (2019), 11 descendants of its own
- K193550: Therm-X (2020), 10 descendants of its own

## Recalls of this device
- Aug 11, 2010 · Not classified · Z-2656-2010: Covidien issued an Urgent Product Recall of the Sterile ImPad Rigid Sole Foot Cover. The product is indicated for prevention of blood pooling in the limb. 120 cases of each Lot code 6066 (right foot) 
- Aug 11, 2010 · Not classified · Z-2657-2010: Covidien issued an Urgent Product Recall of the Sterile ImPad Rigid Sole Foot Cover. The product is indicated for prevention of blood pooling in the limb. 120 cases of each Lot code 6066 (right foot) 

Source page: https://510kreport.com/device/K951683
Methodology: https://510kreport.com/methodology