510(k) K162217

LOYON by Oculus Innovative Sciences — Product Code FRO

K162217 is an FDA 510(k) premarket notification submitted by Oculus Innovative Sciences for the device "LOYON". The FDA issued a decision of Substantially Equivalent on March 23, 2017. The device falls under product code FRO (Dressing, Wound, Drug), a Class U device. Oculus Innovative Sciences has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 23, 2017
Date Received
August 8, 2016
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Dressing, Wound, Drug
Device Class
Class U
Regulation Number
Review Panel
SU
Submission Type