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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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