# K980087: Presdure Products Pressure Pads, Models P100, P110, P120, P130, P200, P210, P220, P230, P300, P310, P320, P330

- Pathway: 510(k) (Traditional)
- Applicant: Pressure Products, Inc.
- Decided: Jul 1, 1998 after 173 days
- Product code: DXC (Clamp, Vascular)
- Device class: 2
- Regulation: 21 CFR 870.4450
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Indications for use
The intended use of the Pressure Products Pressure Pad is to temporarily occlude the femoral artery when used in conjunction with the appropriate femoral artery clamp.

Source page: https://510kreport.com/device/K980087
Methodology: https://510kreport.com/methodology