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

LimFlow V-Ceiver

K Number: K222083 · Decision Aug 9, 2022
Classifications
1
FEI Numbers
36
Registration Numbers
36
Same Product Code
31
Applicant Total
6
Review Days
25

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Basic Information

Device Name
LimFlow V-Ceiver
K Number
K222083
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.5150
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
LimFlow, Inc.
Date Received
July 15, 2022
Decision Date
August 9, 2022
Product Code
MMX
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
Y

Classifications

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

Product Code Device Name
MMX Device, Percutaneous Retrieval

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (MMX), 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
K221902 LimFlow Vector
K221541 LimFlow ARC