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510(k) K861952

COMPOUND LEVERAGE SNIP by Med-Tool, Inc.

K861952 is an FDA 510(k) premarket notification submitted by Med-Tool, Inc. for the device "COMPOUND LEVERAGE SNIP". The FDA issued a decision of Substantially Equivalent on June 6, 1986. Med-Tool, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 6, 1986
Date Received
May 20, 1986
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Other clearances by Med-Tool, Inc.

  • K874357 — TAPERED PUNCH (November 23, 1987)
  • K874358 — COMBINATION WRENCHES (November 23, 1987)
  • K874359 — ADJUSTABLE WRENCHES (November 23, 1987)
  • K874356 — PIN PUNCH (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