Atlas FDA

PARALLEL ACTION PLIERS

FDA 510(k) clearance K861953 · decided 1986-06-06

Clearance details

K-number
K861953
Device name
PARALLEL ACTION PLIERS
Applicant
Med-Tool, Inc.
Decision
Substantially Equivalent
Date received
1986-05-20
Decision date
1986-06-06
Days to decision
17 days
Clearance type
Traditional
Product code
HTC
Device class
1
Regulation number
878.4800
Medical specialty
General, Plastic Surgery
Advisory committee
General, Plastic Surgery
Location
St. Louis, MO, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
SIDE CUTTING PARALLEL ACTION PLIERS (K872384)Med-Tool, Inc.1987-07-02
NEEDLE NOSE PLIERS (K864019)Med-Tool, Inc.1986-10-30
WIRE CUTTING PLIERS OR LINEMAN'S PLIERS (K854390)Med-Tool, Inc.1985-11-19
SLIP JOINT PLIERS (K844600)Med-Tool, Inc.1984-12-14
TOGGLE LOCKING PLIERS-STRAIGHT JAW, CURVED JAW (K844146)Med-Tool, Inc.1984-11-20
SLIP JOINT PLIER (K840979)Med-Tool, Inc.1984-04-25
HALF ROUND FILE (K840980)Med-Tool, Inc.1984-04-25
TOGGLE LOCKING PLIER (K840978)Med-Tool, Inc.1984-04-25
WIRE TWISTERS (K830721)The Anspach Effort, Inc.1983-04-12

Recalls involving this device

No recalls on record reference this clearance.