510(k) K864017

SLOTTED PUNCH by Med-Tool, Inc.

K864017 is an FDA 510(k) premarket notification submitted by Med-Tool, Inc. for the device "SLOTTED PUNCH". The FDA issued a decision of Substantially Equivalent on October 30, 1986. Med-Tool, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 30, 1986
Date Received
October 15, 1986
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No