Goldway Us, Inc. is one of 19121 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Goldway Us, Inc. - FDA 510(k) Cleared Devices
Recent clearances: COMEN MULTI-PARAMETER PATIENT MONITOR, GOLDWAY UT4000A VITAL SIGNS MONITOR, GOLDWAY PATIENT MONITOR, MODEL # UT4000F
4
Total
4
Cleared
0
Denied
Goldway Us, Inc. has 4 FDA 510(k) cleared medical devices. Based in San Jose, US.
Historical record: 4 cleared submissions from 2003 to 2012. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Goldway Us, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Goldway (Us), Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Goldway Us, Inc.
4 devices
Cleared
Nov 07, 2012
COMEN MULTI-PARAMETER PATIENT MONITOR
Cardiovascular
404d
Cleared
Feb 25, 2004
GOLDWAY UT4000A VITAL SIGNS MONITOR
Cardiovascular
64d
Cleared
Apr 11, 2003
GOLDWAY PATIENT MONITOR, MODEL # UT4000F
Cardiovascular
366d
Cleared
Feb 10, 2003
GOLDWAY DIGITAL VIDEO COLPOSCOPE IMAGING SYSTEM, MODEL #SLC-2000
Obstetrics & Gynecology
306d