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PCI Medical Announces 510(k) Submission to FDA for Automated Reprocessors for Endovaginal/Endorectal Probes and TEE Probes

2015-04-02 12:31:11| Industrial Newsroom - All News for Today

PCI Medical announces that it has submitted the GUS ASTRA VR and GUS ASTRA TEE to the U.S. Food and Drug Administration (FDA) for 510(k) clearance, and that the submission is now in substantive review. The GUS ASTRA VR is an automated reprocessor for the high-level disinfection of endovaginal/endorectal...

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