510(k) K930178
K930178 is an FDA 510(k) premarket notification submitted by Arizona Implant Dentistry for the device "ELECTRO FLOSS". The FDA issued a decision of Substantially Equivalent on July 28, 1993. The device falls under product code JET (Pick, Massaging), a Class I device regulated under 21 CFR 872.6650.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 28, 1993
- Date Received
- January 13, 1993
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Pick, Massaging
- Device Class
- Class I
- Regulation Number
- 872.6650
- Review Panel
- DE
- Submission Type