510(k) K761067
K761067 is an FDA 510(k) premarket notification submitted by Ransom and Randolph for the device "DENTSPLY DIE STONE". The FDA issued a decision of Substantially Equivalent on November 30, 1976. Ransom and Randolph has at least 6 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- November 30, 1976
- Date Received
- November 18, 1976
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No