Infrared Laboratory Systems dba SYNERMED
United Statesfrom the FDA registration address FDA establishment FEI 3003593973
- Devices
- 3
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
Synermed Opiate Enzyme Immunoassay Ref K172416
Regimes: 510(k) Registry: 510(k)Synermed ISE Reagents Ref K181201
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3003593973
- Address
- 17408 Tiller Ct Ste 1900, WESTFIELD, IN, 46074
Frequently asked questions
How many devices does Infrared Laboratory Systems dba SYNERMED have in the registry?
The registry currently lists 3 devices for Infrared Laboratory Systems dba SYNERMED. Devices recorded under merged duplicate company entries are counted once.
Which registries list Infrared Laboratory Systems dba SYNERMED's devices?
Among its 3 most recently registered devices, Infrared Laboratory Systems dba SYNERMED has devices listed in FDA 510(k) (3 devices).
What risk classes do Infrared Laboratory Systems dba SYNERMED's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Infrared Laboratory Systems dba SYNERMED's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Infrared Laboratory Systems dba SYNERMED in the registry?
The most recently registered devices listed for Infrared Laboratory Systems dba SYNERMED include Synermed Opiate Enzyme Immunoassay, Synermed ISE Reagents and Synermed Glucose Reagent, Synermed IR-1200 Chemistry Analyzer.