510(k) K102778

CELLAVISION DM1200 WITH THE BODY FLUID APPLICTION by CellaVision AB — Product Code JOY

K102778 is an FDA 510(k) premarket notification submitted by CellaVision AB for the device "CELLAVISION DM1200 WITH THE BODY FLUID APPLICTION". The FDA issued a decision of Substantially Equivalent on September 16, 2011. The device falls under product code JOY (Device, Automated Cell-Locating), a Class II device regulated under 21 CFR 864.5260. CellaVision AB has at least 6 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 16, 2011
Date Received
September 24, 2010
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Device, Automated Cell-Locating
Device Class
Class II
Regulation Number
864.5260
Review Panel
HE
Submission Type