FDA 510(k) Applications Submitted by GOLDWAY (US), INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K112877 | 09/30/2011 | COMEN MULTI-PARAMETER PATIENT MONITOR | GOLDWAY (US), INC. |
| K033988 | 12/23/2003 | GOLDWAY UT4000A VITAL SIGNS MONITOR | GOLDWAY (US), INC. |
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