510(k) K002067

RADIANALYZER, MODEL 12710 by Radi Medical Systems AB — Product Code DSK

K002067 is an FDA 510(k) premarket notification submitted by Radi Medical Systems AB for the device "RADIANALYZER, MODEL 12710". The FDA issued a decision of Substantially Equivalent on January 11, 2001. The device falls under product code DSK (Computer, Blood-Pressure), a Class II device regulated under 21 CFR 870.1110. Radi Medical Systems AB has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 11, 2001
Date Received
July 7, 2000
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Computer, Blood-Pressure
Device Class
Class II
Regulation Number
870.1110
Review Panel
CV
Submission Type