510(k) K926083

NUCLEAR PATIENT SANNING TABLES, VARIOUS TYPES by Biodan Medical Systems, Ltd. — Product Code IYX

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 12, 1993
Date Received
December 1, 1992
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Camera, Scintillation (Gamma)
Device Class
Class I
Regulation Number
892.1100
Review Panel
RA
Submission Type