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

Firefighter™ NC Pro PTCA Balloon Catheter

K Number: K223189 · Decision Jul 21, 2023
Classifications
1
FEI Numbers
76
Registration Numbers
76
Same Product Code
85
Applicant Total
3
Review Days
282

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Basic Information

Device Name
Firefighter™ NC Pro PTCA Balloon Catheter
K Number
K223189
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.5100
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Shanghai MicroPort Medical (Group) Co., Ltd.
Date Received
October 12, 2022
Decision Date
July 21, 2023
Product Code
LOX
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
LOX Catheters, Transluminal Coronary Angioplasty, Percutaneous

Similar 510(k) Clearances

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

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Other Clearances by Shanghai MicroPort Medical (Group) Co., Ltd.

K Number Device Name
K252116 Firefighter™ Pro PTCA Balloon Catheter
K143160 FOXTROT NC PTCA Balloon Catheter