510(k) K823808

VARIOUS ARM SLING by Danek Medical, Inc. — Product Code ILI

K823808 is an FDA 510(k) premarket notification submitted by Danek Medical, Inc. for the device "VARIOUS ARM SLING". The FDA issued a decision of Substantially Equivalent on January 14, 1983. The device falls under product code ILI (Sling, Arm), a Class I device regulated under 21 CFR 890.3640. Danek Medical, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 14, 1983
Date Received
December 17, 1982
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Sling, Arm
Device Class
Class I
Regulation Number
890.3640
Review Panel
PM
Submission Type