# K944301: Hudson Rci Lifesaver Single Patient Use Manual Resuscitator Catalog Numbers: 5360 Through 5380

- Pathway: 510(k) (Traditional)
- Applicant: Hudson Respiratory Care, Inc.
- Decided: Dec 21, 1994 after 106 days
- Product code: BTM (Ventilator, Emergency, Manual (Resuscitator))
- Device class: 2
- Regulation: 21 CFR 868.5915
- 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; 2 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
- K082092: Dispo-Bag Manual Resuscitator, Disposable Adjustable Peep Valve, Disposable Fixed Peep Valve (2008), 6 descendants of its own
- K170663: Foremount Disposable PVC Resuscitator, Foremount Disposable PEEP Valve, Foremount Disposable Manometer (2018), 1 descendant of its own
- K090317: Babi*Plus Bubble Pap Valve (2009), 1 descendant of its own
- K210288: Disposable Manual Resuscitator (2021), 0 descendants of its own
- K133957: Disposable Adjustable Peep Valve MR Conditional Use (2014), 0 descendants of its own

Source page: https://510kreport.com/device/K944301
Methodology: https://510kreport.com/methodology