510(k) K152406
K152406 is an FDA 510(k) premarket notification submitted by Forward Science, LLC for the device "SalivaMAX". The FDA issued a decision of Substantially Equivalent on December 23, 2015. The device falls under product code LFD (Saliva, Artificial), a Class U device. Forward Science, LLC has at least 3 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 23, 2015
- Date Received
- August 25, 2015
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Saliva, Artificial
- Device Class
- Class U
- Regulation Number
- Review Panel
- DE
- Submission Type