FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇪 Ireland

Millipede70 Aspiration Catheter; Perfuze Aspiration Tube Set

K Number: K252392 · Decision Aug 29, 2025
Classifications
1
FEI Numbers
59
Registration Numbers
59
Same Product Code
108
Applicant Total
9
Review Days
29

Basic Information

Device Name
Millipede70 Aspiration Catheter; Perfuze Aspiration Tube Set
K Number
K252392
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
870.1250
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Perfuze, Ltd.
Date Received
July 31, 2025
Decision Date
August 29, 2025
Product Code
NRY
Advisory Committee
Cardiovascular
Review Advisory Committee
NE
Third Party
N

Classifications

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

Product Code Device Name
NRY Catheter, Thrombus Retriever

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K231802 Millipede 088 Access Catheter
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