Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Applications Submitted by DIACOUSTIC MEDICAL DEVICES (PTY) LTD.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K110704
03/14/2011
SENSI
DIACOUSTIC MEDICAL DEVICES (PTY) LTD.
K131044
04/15/2013
SENSICARDIAC MOBI DIAGNOSTIC HEART MURMUR APPLICATION
DIACOUSTIC MEDICAL DEVICES (PTY) LTD.
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact