510(k) K770931
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 3, 1977
- Date Received
- May 23, 1977
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Syringe, Restorative And Impression Material
- Device Class
- Class I
- Regulation Number
- 872.4565
- Review Panel
- DE
- Submission Type