Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Applications Submitted by OPKO INSTRUMENTATION, INC
FDA 510(k) Number
Submission Date
Device Name
Applicant
K092837
09/15/2009
OTI-SCAN 3000
OPKO INSTRUMENTATION, INC
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact