FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Esperance Aspiration Catheter System

K Number: K211697 · Decision Nov 16, 2021
Classifications
1
FEI Numbers
59
Registration Numbers
59
Same Product Code
108
Applicant Total
5
Review Days
166

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Basic Information

Device Name
Esperance Aspiration Catheter System
K Number
K211697
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1250
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Wallaby Medical
Date Received
June 3, 2021
Decision Date
November 16, 2021
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 Wallaby Medical

K Number Device Name
K240917 Esperance 3+ Aspiration Catheter System
K231056 Esperance Distal Access Catheter
K232437 Paragon 8F Balloon Guide Catheter
K223139 Wallaby 017 Micro Catheter