510(k) K033193
- Device
- SONOSENS
- Applicant
- FRIENDLY SENSORS AG
- 510(k) number
- K033193
- Product code
- NKI
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 2004-01-23
- Date received
- 2003-10-02
- Regulation
- 888.1500
- Classification name
- Goniometer With Electrodes
- Medical specialty
- Orthopedic
- Review panel
- Neurology
- Device class
- 2
- Clearance type
- Abbreviated
- Statement or summary
- Summary
- Third party reviewed
- No
Related Records
Applicant Contact
- Contact
- TRISH LANDRY
- Address
- 719 A St. NE Washington DC US 20002 20002
FDA Registration Numbers
- 3026042200
- 3027475369
Source Documents
Legacy Summary
summary
FDA Review
Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links Follow FDA En Español Home Food Drugs Medical Devices Radiation-Emitting Products Vaccines, Blood & Biologics Animal & Veterinary Cosmetics Tobacco Products FDA Home Medical Devices Databases