Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Applications Submitted by RICHARD S DILLON
FDA 510(k) Number
Submission Date
Device Name
Applicant
K971026
03/20/1997
THE CIRCULATOR BOOT
CIRCULATOR BOOT CORP.
K082134
07/29/2008
CIRCULATOR BOOT
CIRCULATOR BOOT CORP.
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact