510(k) K162361

Soft Plug Extended Duration 180 Canalicular Plug by Oasis Medical, Inc. — Product Code LZU

K162361 is an FDA 510(k) premarket notification submitted by Oasis Medical, Inc. for the device "Soft Plug Extended Duration 180 Canalicular Plug". The FDA issued a decision of Substantially Equivalent on April 17, 2017. The device falls under product code LZU (Plug, Punctum), a Class U device. Oasis Medical, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 17, 2017
Date Received
August 23, 2016
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Plug, Punctum
Device Class
Class U
Regulation Number
Review Panel
OP
Submission Type