510(k) K980437

SILICONE PUNCTAL PLUG by Oasis Medical, Inc. — Product Code LZU

K980437 is an FDA 510(k) premarket notification submitted by Oasis Medical, Inc. for the device "SILICONE PUNCTAL PLUG". The FDA issued a decision of Substantially Equivalent on April 30, 1998. 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 30, 1998
Date Received
February 4, 1998
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