Intuit Medical Products, LLC
United Statesfrom the FDA registration address FDA establishment FEI 3012422952
- Devices
- 3
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Dillard Airway Dilatation System Ref K153484
Regimes: 510(k) Registry: 510(k)DSS Sinusplasty Balloon Catheter Ref K143738
Regimes: 510(k) Registry: 510(k)Dillard Nasal Balloon Catheter Ref K181546
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3012422952
- Address
- 1990 Riverside Parkway, Lawrenceville, GA, 30043
Frequently asked questions
How many devices does INTUIT MEDICAL PRODUCTS, LLC have in the registry?
The registry currently lists 3 devices for INTUIT MEDICAL PRODUCTS, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list INTUIT MEDICAL PRODUCTS, LLC's devices?
Among its 3 most recently registered devices, INTUIT MEDICAL PRODUCTS, LLC has devices listed in FDA 510(k) (3 devices).
What risk classes do INTUIT MEDICAL PRODUCTS, LLC's devices fall under?
Among its 3 most recently registered devices, the classes recorded for INTUIT MEDICAL PRODUCTS, LLC's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from INTUIT MEDICAL PRODUCTS, LLC in the registry?
The most recently registered devices listed for INTUIT MEDICAL PRODUCTS, LLC include Dillard Airway Dilatation System, DSS Sinusplasty Balloon Catheter and Dillard Nasal Balloon Catheter.