# K982020: Metron QA-Ids I.V. Pump Tester

- Pathway: 510(k) (Traditional)
- Applicant: Metron U.S., Inc.
- Decided: Sep 30, 1998 after 113 days
- Product code: FRN (Pump, Infusion)
- Device class: 2
- Regulation: 21 CFR 880.5725
- 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 Metron QA-IDS Infusion Pump-Tester is designed for use by trained service technicians, for testing all types of infusion-pumps. Tests include volumetric tests, bolus tests, and occlusion tests. The Metron QA-IDS Infusion Pump Tester is designed to be used by trained service technicians.

Source page: https://510kreport.com/device/K982020
Methodology: https://510kreport.com/methodology