# K001025: Lifecard CF Compact Recorder

- Pathway: 510(k) (Special)
- Applicant: Reynolds Medical, Ltd.
- Decided: Apr 19, 2000 after 20 days
- Product code: DSH (Recorder, Magnetic Tape, Medical)
- Device class: 2
- Regulation: 21 CFR 870.2800
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
8 later devices descend from it; 3 cite it directly.
0 of 9 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
- K071085: E3-80 Portable Ecg Recorder & Analyzer (2007), 3 descendants of its own
- K101569: V-Trust Model TD-2202 Portable Ecg Recorder (2011), 2 descendants of its own
- K011837: Lifecard CF 7 Day (2001), 2 descendants of its own
- K212317: Eclipse MINI Model 98900 (2022), 0 descendants of its own
- K211651: Eclipse PRO (2021), 0 descendants of its own

Source page: https://510kreport.com/device/K001025
Methodology: https://510kreport.com/methodology