12 results
·
23ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
CavaClear Laser Sheath
FDA 510(k)
FDA Class 2
·Cardiovascular
CAVACLEAR LASER SHEATH
FDA Adverse Event
Malfunction
·PHILIPS IMAGE GUIDED THERAPY CORPORATION·Product code QRJ·August 6, 2024
CAVACLEAR LASER SHEATH
FDA Adverse Event
Malfunction
·PHILIPS IMAGE GUIDED THERAPY CORPORATION·Product code QRJ·November 14, 2025
CAVACLEAR LASER SHEATH
FDA Adverse Event
Malfunction
·PHILIPS IMAGE GUIDED THERAPY CORPORATION·Product code QRJ·October 29, 2025
CAVACLEAR LASER SHEATH
FDA Adverse Event
Malfunction
·PHILIPS IMAGE GUIDED THERAPY CORPORATION·Product code QRJ·November 17, 2025
CAVACLEAR LASER SHEATH
FDA Adverse Event
Malfunction
·PHILIPS IMAGE GUIDED THERAPY CORPORATION·Product code QRJ·December 1, 2023
CAVACLEAR LASER SHEATH
FDA Adverse Event
Malfunction
·PHILIPS IMAGE GUIDED THERAPY CORPORATION·Product code QRJ·July 23, 2024
EaseVRx
FDA 510(k)
FDA Class 2
·Neurology
Zuno Smart Sterilization Container
FDA 510(k)
FDA Class 2
·General Hospital
SPECTRANETICS 16F CAVACLEAR LASER SHEATH
FDA Adverse Event
Injury
·THE SPECTRANETICS CORPORATION·Product code QRJ·November 21, 2022
CAVACLEAR LASER SHEATH
FDA Adverse Event
Injury
·PHILIPS IMAGE GUIDED THERAPY CORPORATION·Product code QRJ·February 19, 2025
CAVACLEAR LASER SHEATH
FDA Adverse Event
Injury
·PHILIPS IMAGE GUIDED THERAPY CORPORATION·Product code QRJ·March 5, 2025