510(k) K912816

PRESS 1 PRESS 2 9220 UPDATING OF THE MODULE by S & W Medico Teknik — Product Code DSK

K912816 is an FDA 510(k) premarket notification submitted by S & W Medico Teknik for the device "PRESS 1 PRESS 2 9220 UPDATING OF THE MODULE". The FDA issued a decision of Substantially Equivalent on April 10, 1992. The device falls under product code DSK (Computer, Blood-Pressure), a Class II device regulated under 21 CFR 870.1110. S & W Medico Teknik has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 10, 1992
Date Received
June 18, 1991
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