FDA 510(k) Applications Submitted by GOLDWAY US, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K021153 04/10/2002 GOLDWAY DIGITAL VIDEO COLPOSCOPE IMAGING SYSTEM, MODEL #SLC-2000 GOLDWAY US, INC.
K021154 04/10/2002 GOLDWAY PATIENT MONITOR, MODEL # UT4000F GOLDWAY US, INC.


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