510(k) K180680
K180680 is an FDA 510(k) premarket notification submitted by Laclede, Inc. for the device "Salivea Dry Mouth Mouthwash, Salivea Dry Mouth Mouthspray". The FDA issued a decision of Substantially Equivalent on October 11, 2018. The device falls under product code LFD (Saliva, Artificial), a Class U device. Laclede, Inc. has at least 4 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 11, 2018
- Date Received
- March 15, 2018
- 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