Heathrow Scientific, LLC
United Statesfrom the FDA registration address FDA establishment FEI 3003510542
- Devices
- 5
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
Sharp Chute Ref K091690
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3003510542
- Address
- 440 N Fairway Dr, Vernon Hills, IL, 60061
Frequently asked questions
How many devices does HEATHROW SCIENTIFIC, LLC have in the registry?
The registry currently lists 5 devices for HEATHROW SCIENTIFIC, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list HEATHROW SCIENTIFIC, LLC's devices?
Among its 5 most recently registered devices, HEATHROW SCIENTIFIC, LLC has devices listed in FDA 510(k) (1 device) and FDA GUDID (4 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do HEATHROW SCIENTIFIC, LLC's devices fall under?
Among its 5 most recently registered devices, the classes recorded for HEATHROW SCIENTIFIC, LLC's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from HEATHROW SCIENTIFIC, LLC in the registry?
The most recently registered devices listed for HEATHROW SCIENTIFIC, LLC include Heathrow Scientific OR1201, Heathrow Scientific OR1202, Heathrow Scientific OR1203 and Heathrow Scientific OR1205.