510(k) K852524
K852524 is an FDA 510(k) premarket notification submitted by Spelna, Inc. for the device "SATALEC SERVOTORQUE S2 SX2". The FDA issued a decision of Substantially Equivalent on July 31, 1985. The device falls under product code EIA (Unit, Operative Dental), a Class I device regulated under 21 CFR 872.6640. Spelna, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 31, 1985
- Date Received
- June 14, 1985
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Unit, Operative Dental
- Device Class
- Class I
- Regulation Number
- 872.6640
- Review Panel
- DE
- Submission Type