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

LimFlow Vector

K Number: K221902 · Decision Dec 21, 2022
Classifications
1
FEI Numbers
12
Registration Numbers
12
Same Product Code
26
Applicant Total
6
Review Days
174

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Basic Information

Device Name
LimFlow Vector
K Number
K221902
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.4885
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
LimFlow, Inc.
Date Received
June 30, 2022
Decision Date
December 21, 2022
Product Code
MGZ
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
MGZ Valvulotome

Similar 510(k) Clearances

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

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Other Clearances by LimFlow, Inc.

K Number Device Name
K260188 LimFlow Vector
K251376 LimFlow ARC
K242776 LimFlow V-Ceiver
K221541 LimFlow ARC
K222083 LimFlow V-Ceiver