# K112660: Pocketcpr

- Pathway: 510(k) (Abbreviated)
- Applicant: Zoll Medical Corp
- Decided: May 10, 2012 after 240 days
- Product code: LIX (Aid, Cardiopulmonary Resuscitation)
- Device class: 2
- Regulation: 21 CFR 870.5210
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K071321 (2007). 1 ancestor in all.
1 later device descends from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K071321: Pocketcpr, Bio-Detek, Inc. (2007) Summary page 1.

## Most influential descendants
- K123597: Truecpr Coaching Device (2013), 0 descendants of its own

## Indications for use
To assist users in the performance of effective CPR on a patient 8 years or older.

Source page: https://510kreport.com/device/K112660
Methodology: https://510kreport.com/methodology