FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

ARTHREX TOURNIQUET FOR LEG HOLDER

K Number: K933994 · Decision Mar 23, 1994
Classifications
1
FEI Numbers
107
Registration Numbers
107
Same Product Code
33
Applicant Total
348
Review Days
218

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
ARTHREX TOURNIQUET FOR LEG HOLDER
K Number
K933994
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.5910
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Arthrex, Inc.
Date Received
August 17, 1993
Decision Date
March 23, 1994
Product Code
KCY
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
KCY Tourniquet, Pneumatic

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (KCY), ordered by most recent decision date.

View all

Other Clearances by Arthrex, Inc.

K Number Device Name
K253931 Arthrex Bioabsorbable PushLock Suture Anchors
K254215 Arthrex Beaming System
K252016 Arthrex Humeral Nails
K260561 Arthrex FiberTak Suture Anchor
K260405 FiberTape Button
K252196 Arthrex FibuLock Nail System
K260353 Arthrex Humeral Plating System (Anatomic Humeral Plate) and Cerclage Button
K254229 Arthrex Nano FiberTak Suture Anchor
K253713 Arthrex Variable Angle (VA) Proximal Tibia Plating System
K252807 Arthrex Anatomic Lapidus Plates and I-Beam Lapidus Plates
Search all 348 clearances from Arthrex, Inc. →