Home › PCI Medical Announces FDA 510(k) Clearance for ASTRA VR and ASTRA TEE Automated Reprocessors for Endovaginal/Endorectal Probes and TEE Ultrasound Probes
 

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PCI Medical Announces FDA 510(k) Clearance for ASTRA VR and ASTRA TEE Automated Reprocessors for Endovaginal/Endorectal Probes and TEE Ultrasound Probes

2015-11-25 11:31:10| Industrial Newsroom - All News for Today

Deep River, Connecticut PCI Medical is pleased to announce that it has received 510(k) clearance from the U.S. Food and Drug Administration for the ASTRA VR and ASTRA TEE automated reprocessors used to facilitate the high-level disinfection of endocavity ultrasound probes. "The ASTRA VR and ASTRA TEE automated...

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