# K965172: Oximeter Pre-Amp Cable

- Pathway: 510(k) (Traditional)
- Applicant: Epic Medical Equipment Services, Inc.
- Decided: Jul 16, 1997 after 204 days
- Product code: DQA (Oximeter)
- Device class: 2
- Regulation: 21 CFR 870.2700
- 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
Replacement for Nellcor® Patient Module; to connect oximeter sensors to oximeter monitor. For use with Nellcor® N200® and N100® 5 button oximeters only.

Source page: https://510kreport.com/device/K965172
Methodology: https://510kreport.com/methodology