510(k) K981693
K981693 is an FDA 510(k) premarket notification submitted by Gebauer Co. for the device "SALIVART ORAL MOISTURIZER MODEL NUMBER 03866-009-75 SALIVART ORAL MOISTURIZER MODEL NUMBER 0386-000-25". The FDA issued a decision of Substantially Equivalent on August 6, 2001. The device falls under product code LFD (Saliva, Artificial), a Class U device. Gebauer Co. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 6, 2001
- Date Received
- May 13, 1998
- 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