FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

SUPER SHEATH INTRODUCER SHEATH AND SUPER SHEATH INTRODUCER SHEATH SETS

K Number: K121504 · Decision Sep 27, 2012
Classifications
1
FEI Numbers
273
Registration Numbers
273
Same Product Code
701
Applicant Total
17
Review Days
129

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Basic Information

Device Name
SUPER SHEATH INTRODUCER SHEATH AND SUPER SHEATH INTRODUCER SHEATH SETS
K Number
K121504
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1340
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Togo Medikit Co., Ltd.
Date Received
May 21, 2012
Decision Date
September 27, 2012
Product Code
DYB
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
DYB Introducer, Catheter

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
K141070 SUPER SHEATH
K140419 SUPERCATH5
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. →