# K973843: Msi Pressure Infusor

- Pathway: 510(k) (Traditional)
- Applicant: Smith Assoc.
- Decided: Oct 29, 1997 after 21 days
- Product code: KZD (Infusor, Pressure, For I.V. Bags)
- Device class: 1
- Regulation: 21 CFR 880.5420
- 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 Medical Solutions, Inc.’s Reusable Pressure Infusor is a device consisting of an inflatable cuff which is placed around an I.V. bag. When the device is inflated, it increases the pressure on the I.V. bag to assist the infusion of fluid. Caution: Federal (U.S.A) law restricts this device to sale by or on the order of a physician.

Source page: https://510kreport.com/device/K973843
Methodology: https://510kreport.com/methodology