# K963717: Millex - MP Filter Unit (SLMPO25SS/SLMPL25SS)

- Pathway: 510(k) (Traditional)
- Applicant: Millipore Corp.
- Decided: Jun 10, 1997 after 267 days
- Product code: BSN (Filter, Conduction, Anesthetic)
- Device class: 2
- Regulation: 21 CFR 868.5130
- 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
For use as a syringe filter to sterilize/ultraclean low volume solutions in direct patient care and pharmacy admixture applications.

Source page: https://510kreport.com/device/K963717
Methodology: https://510kreport.com/methodology