# K892885: Resubmitted RD1000 Neopuff Infant Resuscitator

- Pathway: 510(k) (Traditional)
- Applicant: Fisher & Paykel Electronics, Ltd.
- Decided: Oct 6, 1989 after 170 days
- Product code: BTL (Ventilator, Emergency, Powered (Resuscitator))
- Device class: 2
- Regulation: 21 CFR 868.5925
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
26 later devices descend from it; 12 cite it directly.
6 of 27 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
- K070210: Giraffe and Panda  T- Piece Resuscitation System (2007), 10 descendants of its own
- K092085: Ispira Resuscitation Unit (2009), 4 descendants of its own
- K072021: Neopip Infant Resuscitator (2007), 3 descendants of its own
- K070377: Giraffe and Panda Warmer (2007), 3 descendants of its own
- K120642: Resuscitaire with Autobreath (2012), 2 descendants of its own

Source page: https://510kreport.com/device/K892885
Methodology: https://510kreport.com/methodology