FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇳 China

JADE PLUS PTA Balloon Dilatation Catheter

K Number: K241025 · Decision Jun 11, 2024
Classifications
1
FEI Numbers
92
Registration Numbers
92
Same Product Code
402
Applicant Total
9
Review Days
57

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Basic Information

Device Name
JADE PLUS PTA Balloon Dilatation Catheter
K Number
K241025
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1250
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
OrbusNeich Medical (Shenzhen) Co., Ltd.
Date Received
April 15, 2024
Decision Date
June 11, 2024
Product Code
LIT
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
LIT Catheter, Angioplasty, Peripheral, Transluminal

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Other Clearances by OrbusNeich Medical (Shenzhen) Co., Ltd.

K Number Device Name
K253361 Teleport Glide Microcatheter
K242588 COREPASS Modular Microcatheter (FLEX); COREPASS Modular Microcatheter (CONTROL)
K233499 Sapphire NC ULTRA Coronary Dilatation Catheter
K233505 Sapphire ULTRA Coronary Dilatation Catheter
K231608 Teleport XT Microcatheter
K211807 Sapphire NC 24
K202231 JADE
K201794 Jade