510(k) K812646

SKI 5000 by Smithkline Diagnostics, Inc. — Product Code DXK

K812646 is an FDA 510(k) premarket notification submitted by Smithkline Diagnostics, Inc. for the device "SKI 5000". The FDA issued a decision of Substantially Equivalent on November 16, 1981. The device falls under product code DXK (Echocardiograph), a Class II device regulated under 21 CFR 870.2330. Smithkline Diagnostics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 16, 1981
Date Received
September 17, 1981
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Echocardiograph
Device Class
Class II
Regulation Number
870.2330
Review Panel
CV
Submission Type