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

Millipede 088 Access Catheter; Millipede 070 Aspiration Catheter; Perfuze Aspiration Tube Set

K Number: K242504 · Decision Sep 20, 2024
Classifications
1
FEI Numbers
59
Registration Numbers
59
Same Product Code
108
Applicant Total
9
Review Days
29

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Basic Information

Device Name
Millipede 088 Access Catheter; Millipede 070 Aspiration Catheter; Perfuze Aspiration Tube Set
K Number
K242504
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
August 22, 2024
Decision Date
September 20, 2024
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

Similar 510(k) Clearances

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

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Other Clearances by Perfuze, Ltd.

K Number Device Name
K253590 Millipede System
K252392 Millipede70 Aspiration Catheter; Perfuze Aspiration Tube Set
K250012 Millipede 070 Aspiration Catheter; Perfuze Aspiration Tube Set
K240711 Zipline Access Catheter
K233648 Millipede 088 Access Catheter
K232524 Millipede 070 Aspiration Catheter; Perfuze Aspiration Tube Set
K231802 Millipede 088 Access Catheter
K214048 Millipede 088 Access Catheter