510(k) K935440
K935440 is an FDA 510(k) premarket notification submitted by Johnson & Johnson Consumer Products, Inc. for the device "JOHNSON & JOHNSON FLUORIDE DENTAL FLOSS, MINT WAXED". The FDA issued a decision of Substantially Equivalent on February 3, 1994. The device falls under product code JES (Floss, Dental), a Class I device regulated under 21 CFR 872.6390. Johnson & Johnson Consumer Products, Inc. has at least 7 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- February 3, 1994
- Date Received
- November 12, 1993
- 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