Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Applications Submitted by WAYNE V LOOMER
FDA 510(k) Number
Submission Date
Device Name
Applicant
K960998
03/12/1996
XRE COLLIMATOR
XRE CORP.
K961193
03/21/1996
FULL FRAME ZOOM SYSTEM
XRE CORP.
K973744
10/01/1997
UNICATH SP BI-PLANE (MODEL M269 & M289)
XRE CORP.
K984414
12/10/1998
XRE COLLIMATOR WITH SPECTRAL FILTER
TREX MEDICAL CORP.
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact