Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Applications Submitted by APPLIED CARDIAC SYSTEMS, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K103706
12/20/2010
THE CORE (CARDIAC OUTPATIENT REALTIME ECG) MONITOR
APPLIED CARDIAC SYSTEMS, INC.
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact