510(k) K862752
K862752 is an FDA 510(k) premarket notification submitted by Protek, Inc. for the device "C.S.M. HIP". The FDA issued a decision of Substantially Equivalent on August 7, 1986. Protek, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 7, 1986
- Date Received
- July 22, 1986
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No