510(k) K972879

ULTRAFAST CT SCANNER; EBT CT SCANNER, EVOLUTION by Imatron, Inc. — Product Code JAK

K972879 is an FDA 510(k) premarket notification submitted by Imatron, Inc. for the device "ULTRAFAST CT SCANNER; EBT CT SCANNER, EVOLUTION". The FDA issued a decision of Substantially Equivalent on October 15, 1997. The device falls under product code JAK (System, X-Ray, Tomography, Computed), a Class II device regulated under 21 CFR 892.1750. Imatron, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 15, 1997
Date Received
August 5, 1997
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
System, X-Ray, Tomography, Computed
Device Class
Class II
Regulation Number
892.1750
Review Panel
RA
Submission Type