510(k) K961163
K961163 is an FDA 510(k) premarket notification submitted by Lares Research, Inc. for the device "LARES RESEARCH AS-1 LOWSPEED HANDPIECE". The FDA issued a decision of Substantially Equivalent on April 23, 1996. The device falls under product code EFB (Handpiece, Air-Powered, Dental), a Class I device regulated under 21 CFR 872.4200. Lares Research, Inc. has at least 9 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- April 23, 1996
- Date Received
- March 22, 1996
- 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