510(k) K983547
K983547 is an FDA 510(k) premarket notification submitted by Protech, Inc. for the device "PROTECH PLUS". The FDA issued a decision of Substantially Equivalent on Jan 7, 1999. The device falls under product code EBI (Resin, Denture, Relining, Repairing, Rebasing), a Class II device regulated under 21 CFR 872.3760.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Jan 7, 1999
- Date Received
- Oct 9, 1998
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Resin, Denture, Relining, Repairing, Rebasing
- Device Class
- Class II
- Regulation Number
- 872.3760
- Review Panel
- DE
- Submission Type
- 510(k)