510(k) K971350
K971350 is an FDA 510(k) premarket notification submitted by Micro-Mega Societe Anonyme for the device "SERIES XE, SERIES SE, SERIES TE". The FDA issued a decision of Substantially Equivalent on June 4, 1997. The device falls under product code EGS (Handpiece, Contra- And Right-Angle Attachment, Dental), a Class I device regulated under 21 CFR 872.4200. Micro-Mega Societe Anonyme has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 4, 1997
- Date Received
- April 10, 1997
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Handpiece, Contra- And Right-Angle Attachment, Dental
- Device Class
- Class I
- Regulation Number
- 872.4200
- Review Panel
- DE
- Submission Type