510(k) K791852
K791852 is an FDA 510(k) premarket notification submitted by Mem Medical, Inc. for the device "T-PC FOR R.F. M.D., M-501". The FDA issued a decision of Substantially Equivalent on October 1, 1979. Mem Medical, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 1, 1979
- Date Received
- September 19, 1979
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No