# K935662: Synermed IR 500 Chemistry Analyzer

- Pathway: 510(k) (Traditional)
- Applicant: Synermed, Inc.
- Decided: Apr 26, 1994 after 151 days
- Product code: JIQ (Turbidimetric Method, Protein Or Albumin (Urinary, Non-Quant.))
- Device class: 1
- Regulation: 21 CFR 862.1645
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K974779: Abbott Alcyon (TM) 300 (Without Ise Module) and 300I (with Ise Module) Analyzer (1998), 0 descendants of its own

Source page: https://510kreport.com/device/K935662
Methodology: https://510kreport.com/methodology