510(k) K983551

CRIT-SCAN II MONITOR by In-Line Diagnostics Corp. — Product Code GKF

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 27, 1999
Date Received
October 9, 1998
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Instrument, Hematocrit, Automated
Device Class
Class II
Regulation Number
864.5600
Review Panel
HE
Submission Type