Medical Device Manufacturer · US , Cardiff By The Sea , CA

Atraverse Medical - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2024
2
Total
2
Cleared
0
Denied
FDA 510(k) Regulatory Record - Atraverse Medical Cardiovascular ✕
2 devices
1-2 of 2
Cleared Feb 27, 2026
HOTWIRE RF GUIDEWIRE (901XXX)
K260292 · DXF
Cardiovascular · 29d
Cleared May 01, 2024
HOTWIRE™ RF Guidewire
K240900 · DXF
Cardiovascular · 30d
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