Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K023020
Device Classification Name
Cassette, Radiographic Film
More FDA Info for this Device
510(K) Number
K023020
Device Name
Cassette, Radiographic Film
Applicant
AGFA CORP.
10 SOUTH ACADEMY ST.
GREENVILLE, SC 29601 US
Other 510(k) Applications for this Company
Contact
PAMELA K GWYNN
Other 510(k) Applications for this Contact
Regulation Number
892.1850
More FDA Info for this Regulation Number
Classification Product Code
IXA
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
09/11/2002
Decision Date
09/26/2002
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
Y
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact