Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K973039
Device Classification Name
Table, Radiographic, Tilting
More FDA Info for this Device
510(K) Number
K973039
Device Name
Table, Radiographic, Tilting
Applicant
GE MEDICAL SYSTEMS
P.O. BOX 414
MILWAUKEE, WI 53201 US
Other 510(k) Applications for this Company
Contact
LARRY A KROGER
Other 510(k) Applications for this Contact
Regulation Number
892.1980
More FDA Info for this Regulation Number
Classification Product Code
IXR
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
08/14/1997
Decision Date
10/16/1997
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
RA - Radiology
Review Advisory Committee
RA - Radiology
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact