FDA 510(k) Applications Submitted by PCI MEDICAL, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K150504 02/26/2015 GUS ASTRA TEE Transesophageal Probe Reprocessor, GUS ASTRA VR Endovaginal/Endorectal Probe Reprocessor PCI MEDICAL, INC.


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