# Fenem, Inc.

- Location (FDA's records): New York, NY
- FDA decisions: 5 (1988–1989): 5 510(k) clearances
- Product codes: CCK (5)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 5 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Engineered Medical Systems: 2 (https://510kreport.com/company/engineered-medical-systems)
- Nellcor Puritan Bennett, Inc.: 1 (https://510kreport.com/company/nellcor-puritan-bennett)
- Kendall: 1 (https://510kreport.com/company/kendall)
- Mercury Medical: 1 (https://510kreport.com/company/mercury-medical)

## Its most-cited devices
- K894053: 2ND Modification of Fef (TM) End-Tidal CO2 Detector (1989), cited by 5

## Recent decisions
- K894429: Modified Claims for Fef (TM) End-Tidal CO2 Detector (Sep 18, 1989)
- K894053: 2ND Modification of Fef (TM) End-Tidal CO2 Detector (Jul 20, 1989)
- K884080: Modified Fef (TM) End-Tidal CO2 Detector (Oct 21, 1988)
- K883950: Modified Toob-Cheq Carbon Dioxide Gas Analyzer (Sep 29, 1988)
- K883821: Fef (TM) End-Tidal CO2 Detector (Sep 26, 1988)

Source page: https://510kreport.com/company/fenem