510(k) K923350

CLOSED CHAIN ATTACHMENT, MODEL #820-520 by Biodan Medical Systems, Ltd. — Product Code IKK

K923350 is an FDA 510(k) premarket notification submitted by Biodan Medical Systems, Ltd. for the device "CLOSED CHAIN ATTACHMENT, MODEL #820-520". The FDA issued a decision of Substantially Equivalent on July 23, 1992. The device falls under product code IKK (System, Isokinetic Testing And Evaluation), a Class II device regulated under 21 CFR 890.1925. Biodan Medical Systems, Ltd. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 23, 1992
Date Received
July 8, 1992
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
System, Isokinetic Testing And Evaluation
Device Class
Class II
Regulation Number
890.1925
Review Panel
PM
Submission Type