Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K001321
Device Classification Name
Processor, Radiographic-Film, Automatic
More FDA Info for this Device
510(K) Number
K001321
Device Name
Processor, Radiographic-Film, Automatic
Applicant
ALL-PRO IMAGING CORP.
70 CANTIAGUE ROCK RD.
P.O. BOX 870
HICKSVILLE, NY 11801 US
Other 510(k) Applications for this Company
Contact
JOSEPH CAREY
Other 510(k) Applications for this Contact
Regulation Number
892.1900
More FDA Info for this Regulation Number
Classification Product Code
IXW
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
04/26/2000
Decision Date
05/16/2000
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
RA - Radiology
Review Advisory Committee
RA - Radiology
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact