Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
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.
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact