510(k) K983024

PROTON THERAPY SYSTEM by Ion Beam Applications S.A. — Product Code LHN

K983024 is an FDA 510(k) premarket notification submitted by Ion Beam Applications S.A. for the device "PROTON THERAPY SYSTEM". The FDA issued a decision of Substantially Equivalent on July 12, 2001. The device falls under product code LHN (System, Radiation Therapy, Charged-Particle, Medical), a Class II device regulated under 21 CFR 892.5050. Ion Beam Applications S.A. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 12, 2001
Date Received
August 31, 1998
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
System, Radiation Therapy, Charged-Particle, Medical
Device Class
Class II
Regulation Number
892.5050
Review Panel
RA
Submission Type