# K924626: Novametrix Model 510

- Pathway: 510(k) (Traditional)
- Applicant: Novametrix Medical Systems, Inc.
- Decided: Dec 3, 1993 after 445 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.
59 later devices descend from it; 2 cite it directly.
1 of 60 devices in its family (counting itself) has a Class I recall.

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

## Most influential descendants
- K032971: Tidal Wave SP Model 710/715                                       and 715 (2004), 57 descendants of its own
- K083821: Vital Signs Monitor (2009), 39 descendants of its own
- K093016: Vital Signs Monitor (2010), 16 descendants of its own
- K113623: Patient Monitor (2012), 15 descendants of its own
- K042601: Capnostat 5 (2004), 15 descendants of its own

Source page: https://510kreport.com/device/K924626
Methodology: https://510kreport.com/methodology