510(k) K851777
K851777 is an FDA 510(k) premarket notification submitted by Artiberia for the device "23-100 TO 23-124 VARIOUS TYPES OF PROBES". The FDA issued a decision of Substantially Equivalent on Jun 20, 1985. Artiberia has 78 other 510(k) clearances on record.
Clearance details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Jun 20, 1985
- Date Received
- Apr 25, 1985
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No