SIDE CUTTING PARALLEL ACTION PLIERS— 510(k) K872384

Name: FDA 510(k) clearance K872384
Creator: U.S. Food and Drug Administration
Published: 1987-07-02

Substantially Equivalent

Med-Tool, Inc.

FDA 510(k) clearance K872384 for SIDE CUTTING PARALLEL ACTION PLIERS, Substantially Equivalent on 1987-07-02. Applicant: Med-Tool, Inc.. Device class: 1.

Clearance details

Applicant: Med-Tool, Inc.
Product code: Code HTC
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1987-06-19
Decision date: 1987-07-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: St. Louis, MO, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code HTC

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K864019 — NEEDLE NOSE PLIERS1986-10-30
K861953 — PARALLEL ACTION PLIERS1986-06-06
K854390 — WIRE CUTTING PLIERS OR LINEMAN'S PLIERS1985-11-19
K844600 — SLIP JOINT PLIERS1984-12-14
K844146 — TOGGLE LOCKING PLIERS-STRAIGHT JAW, CURVED JAW1984-11-20

More clearances from Med-Tool, Inc.

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K874356 — PIN PUNCH1987-11-23
K874357 — TAPERED PUNCH1987-11-23
K874358 — COMBINATION WRENCHES1987-11-23
K874359 — ADJUSTABLE WRENCHES1987-11-23
K872388 — NAIL SET1987-07-23

Data sourced from openFDA. This site is unofficial and independent of the FDA.