Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K022708
Device Classification Name
Accelerator, Linear, Medical
More FDA Info for this Device
510(K) Number
K022708
Device Name
Accelerator, Linear, Medical
Applicant
LARSON PRODUCTS, INC.
2844 BANWICK RD.
COLUMBUS, OH 43232-2115 US
Other 510(k) Applications for this Company
Contact
PETER M LARSON
Other 510(k) Applications for this Contact
Regulation Number
892.5050
More FDA Info for this Regulation Number
Classification Product Code
IYE
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
08/14/2002
Decision Date
11/12/2002
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
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact