# K071321: Pocketcpr

- Pathway: 510(k) (Traditional)
- Applicant: Bio-Detek, Inc.
- Decided: Sep 12, 2007 after 125 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
No predicates in its family tree.
10 later devices descend from it; 5 cite it directly.
0 of 11 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) CPR Ezy: named in the summary without a submission number

## Most influential descendants
- K122050: Cprmeter CPR Feedback Device (2012), 5 descendants of its own
- K151702: Reusable Full Silicone Cover (2015), 3 descendants of its own
- K173886: CPRmeter 2 CPR Feedback Device (2018), 2 descendants of its own
- K112660: Pocketcpr (2012), 1 descendant of its own
- K201581: CPR Band (2021), 0 descendants of its own

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

Source page: https://510kreport.com/device/K071321
Methodology: https://510kreport.com/methodology