510(k) K091964
K091964 is an FDA 510(k) premarket notification submitted by Procter & Gamble Co. for the device "CREST GLIDE CLINICAL GUM PROTECTION DENTAL FLOSS". The FDA issued a decision of Substantially Equivalent on September 24, 2009. The device falls under product code JES (Floss, Dental), a Class I device regulated under 21 CFR 872.6390. Procter & Gamble Co. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- September 24, 2009
- Date Received
- July 1, 2009
- 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