# K001308: Modification to Zymed Telemetry System, Model Easiview

- Pathway: 510(k) (Special)
- Applicant: Agilent Technologies
- Decided: May 17, 2000 after 22 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.
12 later devices descend from it; 3 cite it directly.
0 of 13 devices in its family (counting itself) have 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
- K031863: Carestation 126S Videophone (2003), 10 descendants of its own
- K052608: Telephone Based BL Healthcare Remote Care Management System (RCMS) (2006), 5 descendants of its own
- K093379: TCX-I-DV Remote Care Management System (2010), 4 descendants of its own
- K033133: Telecare D.R. Server Software System (2004), 3 descendants of its own
- K073710: Intouch Remote Presence Robotic System, Model RP-7 (2008), 2 descendants of its own

Source page: https://510kreport.com/device/K001308
Methodology: https://510kreport.com/methodology