Safetec Of America, Inc.
Country not established FDA establishment FEI 1000159898
- Devices
- 4
- Registrations
- FDA
- FDA recalls
- 0
What Safetec Of America, Inc. makes
The company produces personal protective equipment kits for emergency response, including spill cleanup solutions and CPR mask kits designed for single-use medical or emergency scenarios.
These devices are classified as Class II under FDA regulations and are authorised via 510(k) clearance. The manufacturer is based in the United States.
Catalogue
Ez-Personal Protection Kit Ref K952962
510(k) 510(k)Ez-Personal Protection Kit With Spill Clean Up Ref K960073
510(k) 510(k)- 510(k) 510(k)
Cpr Mask & Related Family Kits Ref K953461
510(k) 510(k)
Company details
- FDA FEI number
- 1000159898
- Address
- 887 Kensington Avenue, BUFFALO, NY, 14215
Frequently asked questions
How many devices does SAFETEC OF AMERICA, INC. have in the registry?
The registry currently lists 4 devices for SAFETEC OF AMERICA, INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list SAFETEC OF AMERICA, INC.'s devices?
Among its 4 most recently registered devices, SAFETEC OF AMERICA, INC. has devices listed in FDA 510(k) (4 devices).
What risk classes do SAFETEC OF AMERICA, INC.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for SAFETEC OF AMERICA, INC.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from SAFETEC OF AMERICA, INC. in the registry?
The most recently registered devices listed for SAFETEC OF AMERICA, INC. include EZ-PERSONAL PROTECTION KIT, EZ-PERSONAL PROTECTION KIT WITH SPILL CLEAN UP, EZ-PERSONAL PROTECTION KIT WITH SPILL CLEAN UP - PLUS and CPR MASK & RELATED FAMILY KITS.