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

SUPERCATH V

K Number: K052267 · Decision Oct 27, 2006
Classifications
1
FEI Numbers
18
Registration Numbers
18
Same Product Code
78
Applicant Total
17
Review Days
434

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Basic Information

Device Name
SUPERCATH V
K Number
K052267
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5540
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Togo Medikit Co., Ltd.
Date Received
August 19, 2005
Decision Date
October 27, 2006
Product Code
FIE
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

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

Product Code Device Name
FIE Needle, Fistula

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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
K121504 SUPER SHEATH INTRODUCER SHEATH AND SUPER SHEATH INTRODUCER SHEATH SETS
K112290 SUPERCATH Z3V
K093546 SUPERCATH 5 MODEL SP120-XX-XX, SP125-XX-XX
Search all 17 clearances from Togo Medikit Co., Ltd. →