510(k) K925409
K925409 is an FDA 510(k) premarket notification submitted by Oral-B Laboratories for the device "ORAL-B DENTAL FLOSS WITH FLUORIDE". The FDA issued a decision of Substantially Equivalent on January 28, 1993. The device falls under product code JES (Floss, Dental), a Class I device regulated under 21 CFR 872.6390. Oral-B Laboratories has at least 7 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 28, 1993
- Date Received
- October 26, 1992
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Floss, Dental
- Device Class
- Class I
- Regulation Number
- 872.6390
- Review Panel
- DE
- Submission Type