# K960587: Cprotector 2000

- Pathway: 510(k) (Traditional)
- Applicant: Certified Safety Mfg., Inc.
- Decided: Jul 21, 1997 after 525 days
- Product code: CBP (Valve, Non-Rebreathing)
- Device class: 2
- Regulation: 21 CFR 868.5870
- 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 K934821 (1994). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K934821: Cprotector, Certified Safety Mfg., Inc. (1994) Summary page 1.

## Indications for use
A physical barrier for mouth to mouth resuscitation between the victim (patient) and the rescuer. This device makes no “guarantee” of disease protection, but it is designed to help protect the rescuer against potentially contaminated secretions and back drafts emanating from the victim while eliminating actual mouth to mouth contact. This device is to be used only by persons trained in CPR and the use of this device. DO NOT USE THIS DEVICE ON INFANTS.

Source page: https://510kreport.com/device/K960587
Methodology: https://510kreport.com/methodology