Medical Device Manufacturer · US , San Jose , CA

LimFlow, Inc. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 2022

Recent clearances: LimFlow Vector, LimFlow ARC, LimFlow V-Ceiver

6
Total
6
Cleared
0
Denied

FDA 510(k) Regulatory Record - LimFlow, Inc. Cardiovascular ✕

6 devices
1-6 of 6
Cleared Mar 18, 2026
LimFlow Vector
K260188 · MGZ
Cardiovascular · 55d
Cleared May 31, 2025
LimFlow ARC
K251376 · PDU
Cardiovascular · 29d
Cleared Feb 14, 2025
LimFlow V-Ceiver
K242776 · MMX
Cardiovascular · 154d
Cleared Dec 21, 2022
LimFlow Vector
K221902 · MGZ
Cardiovascular · 174d
Cleared Aug 31, 2022
LimFlow ARC
K221541 · PDU
Cardiovascular · 96d
Cleared Aug 09, 2022
LimFlow V-Ceiver
K222083 · MMX
Cardiovascular · 25d
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