510(k) K851896

DOUBLE ACTION PIN CUTTER by Med-Tool, Inc.

K851896 is an FDA 510(k) premarket notification submitted by Med-Tool, Inc. for the device "DOUBLE ACTION PIN CUTTER". The FDA issued a decision of Substantially Equivalent on May 21, 1985. Med-Tool, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 21, 1985
Date Received
April 30, 1985
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No