510(k) K884630
K884630 is an FDA 510(k) premarket notification submitted by Med-Dex Intl. for the device "MULTI-PURPOSE HOLDER". The FDA issued a decision of Substantially Equivalent on Nov 22, 1988. Med-Dex Intl. has 3 other 510(k) clearances on record.
Clearance details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Nov 22, 1988
- Date Received
- Nov 7, 1988
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No