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510(k) K864018

HACKSAW by Med-Tool, Inc.

K864018 is an FDA 510(k) premarket notification submitted by Med-Tool, Inc. for the device "HACKSAW". 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

Other clearances by Med-Tool, Inc.

  • K874356 — PIN PUNCH (November 23, 1987)
  • K874357 — TAPERED PUNCH (November 23, 1987)
  • K874359 — ADJUSTABLE WRENCHES (November 23, 1987)
  • K874358 — COMBINATION WRENCHES (November 23, 1987)
  • K872388 — NAIL SET (July 23, 1987)
  • K872387 — STANDARD SCREW DRIVER (July 16, 1987)
  • K872385 — VICE OR BENCH VICE (July 16, 1987)
  • K872389 — PRECISION SCREW DRIVER SET (July 15, 1987)
  • K872384 — SIDE CUTTING PARALLEL ACTION PLIERS (July 2, 1987)
  • K872386 — C CLAMP (July 2, 1987)

FDA data resources