510(k) K780568
K780568 is an FDA 510(k) premarket notification submitted by Hancock Laboratories, Inc. for the device "DURAN FLEXIBLE RING". The FDA issued a decision of Substantially Equivalent on May 26, 1978. Hancock Laboratories, Inc. has at least 4 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 26, 1978
- Date Received
- April 10, 1978
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No