510(k) K945906

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

K945906 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 January 3, 1995. 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
January 3, 1995
Date Received
December 2, 1994
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