Isovac Products LLC
United Statesfrom the FDA registration address FDA establishment FEI 3006076009
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Capsuls, Models 2003-PUR8C, 2004-PVC8C Ref K052798
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3006076009
- Address
- 1306 Enterprise Dr Ste C, ROMEOVILLE, IL, 60446
Frequently asked questions
How many devices does ISOVAC PRODUCTS LLC have in the registry?
The registry currently lists 2 devices for ISOVAC PRODUCTS LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list ISOVAC PRODUCTS LLC's devices?
Among its 2 most recently registered devices, ISOVAC PRODUCTS LLC has devices listed in FDA 510(k) (2 devices).
What risk classes do ISOVAC PRODUCTS LLC's devices fall under?
Among its 2 most recently registered devices, the classes recorded for ISOVAC PRODUCTS LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from ISOVAC PRODUCTS LLC in the registry?
The most recently registered devices listed for ISOVAC PRODUCTS LLC include CAPSULS, MODELS 2003-PUR8C, 2004-PVC8C and ORCA (tm) - Operational Rescue Containment Apparatus.