FDA 510(k) FDA class 2 Substantially Equivalent 🇯🇵 Japan

SUPER SHEATH

K Number: K141070 · Decision Jan 15, 2015
Classifications
1
FEI Numbers
100
Registration Numbers
100
Same Product Code
103
Applicant Total
17
Review Days
265

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Basic Information

Device Name
SUPER SHEATH
K Number
K141070
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1310
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Togo Medikit Co., Ltd.
Date Received
April 25, 2014
Decision Date
January 15, 2015
Product Code
DRE
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

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

Product Code Device Name
DRE Dilator, Vessel, For Percutaneous Catheterization

Similar 510(k) Clearances

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Other Clearances by Togo Medikit Co., Ltd.

K Number Device Name
K241230 Super Sheath Introducer Sheath S-3N5/1005 S-3N7/1006 S-3W5/1007 S-3W7/1008
K200379 Super Sheath
K190001 Supercath 5
K172496 SUPERCATH 5 (26G)
K160592 SUPERCATH 6
K140419 SUPERCATH5
K121504 SUPER SHEATH INTRODUCER SHEATH AND SUPER SHEATH INTRODUCER SHEATH SETS
K112290 SUPERCATH Z3V
K093546 SUPERCATH 5 MODEL SP120-XX-XX, SP125-XX-XX
K081953 SUPERCATH 5
Search all 17 clearances from Togo Medikit Co., Ltd. →