510(k) K810155
K810155 is an FDA 510(k) premarket notification submitted by Medlog GmbH Marketing Services for the device "DOP 84". The FDA issued a decision of Substantially Equivalent on May 1, 1981. Medlog GmbH Marketing Services has at least 4 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 1, 1981
- Date Received
- January 21, 1981
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No