510(k) K812806

KT-1000 DEVICE by Medmetric Corp. — Product Code LYH

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 10, 1981
Date Received
October 6, 1981
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Arthrometer
Device Class
Class I
Regulation Number
890.1615
Review Panel
NE
Submission Type