2 results
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53ms
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Sources: EU EUDAMED, US FDA
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FDA Recall
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AquaBeam Handpiece, Sterile EO, Rx Only, REF: 310301, and 320301, a component of AquaBeam Robotic System. 320301 distributed outside the U.S. Device Description The AQUABEAM Robotic System is intended for use in patients suffering from lower urinary tract symptoms resulting from benign prostatic hyperplasia (BPH).
FDA Recall
Terminated
·PROCEPT BIOROBOTICS CORPORATION·Product code PZP·March 6, 2019
AQUABEAM Handpiece, REF: HP2000, a sterile single-use component of the AQUABEAM Robotic System.
FDA Recall
Open, Classified
·PROCEPT BIOROBOTICS CORPORATION·Product code PZP·July 9, 2021