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

ERIC Retrieval Device

K Number: K211120 · Decision Mar 31, 2022
Classifications
1
FEI Numbers
59
Registration Numbers
59
Same Product Code
108
Applicant Total
85
Review Days
350

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Basic Information

Device Name
ERIC Retrieval Device
K Number
K211120
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1250
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
MicroVention, Inc.
Date Received
April 15, 2021
Decision Date
March 31, 2022
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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