510(k) K872615

IMATRON C-100 ULTRAFAST CT SCANNER by Imatron, Inc. — Product Code JAK

K872615 is an FDA 510(k) premarket notification submitted by Imatron, Inc. for the device "IMATRON C-100 ULTRAFAST CT SCANNER". The FDA issued a decision of Substantially Equivalent on September 23, 1987. 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
September 23, 1987
Date Received
July 6, 1987
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