Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Applications Submitted by ORION DIAGNOSTICA, DIV. ORION CORP.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K971537
04/28/1997
PYLORISET EIA-G (68926)
ORION DIAGNOSTICA, DIV. ORION CORP.
K031607
05/22/2003
ORION DIAGNOSTICA QUIKREAD CRP KIT AND QUIKREAD CRP CONTROL
ORION DIAGNOSTICA, DIV. ORION CORP.
K022176
07/03/2002
ORION DIAGNOSTICA ULTRASENSITIVE CRP KIT, MODEL 68025, & ORION DIAGNOSTICA ULTRASENSITIVE CRP CONTROL, MODEL 68257
ORION DIAGNOSTICA, DIV. ORION CORP.
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact