Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Applications Submitted by EXTERNAL COUNTERPULSATION LAB
FDA 510(k) Number
Submission Date
Device Name
Applicant
K012141
07/10/2001
AECP-A, AUTOMATIC EXTERNAL COUNTERPULSATION DEVICE
EXTERNAL COUNTERPULSATION LAB
K021340
04/26/2002
AECP-A, AUTOMATIC EXTERNAL COUNTERPULSATION DEVICE
EXTERNAL COUNTERPULSATION LAB
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact