510(k) K090725

OCULUS MICROCYN WOUND GEL by Oculus Innovative Sciences, Inc. — Product Code FRO

K090725 is an FDA 510(k) premarket notification submitted by Oculus Innovative Sciences, Inc. for the device "OCULUS MICROCYN WOUND GEL". The FDA issued a decision of Substantially Equivalent on May 20, 2009. The device falls under product code FRO (Dressing, Wound, Drug), a Class U device. Oculus Innovative Sciences, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 20, 2009
Date Received
March 19, 2009
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