510(k) K760794
K760794 is an FDA 510(k) premarket notification submitted by Midwest for the device "FIBER OPTICS HIGH SPEED HANDPIECE". The FDA issued a decision of Substantially Equivalent on October 20, 1976. The device falls under product code EFB (Handpiece, Air-Powered, Dental), a Class I device regulated under 21 CFR 872.4200. Midwest has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 20, 1976
- Date Received
- October 8, 1976
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Handpiece, Air-Powered, Dental
- Device Class
- Class I
- Regulation Number
- 872.4200
- Review Panel
- DE
- Submission Type