510(k) K013613

SOFT PLUG ABSORBABLE PLUG-SA by Oasis Medical, Inc. — Product Code LZU

K013613 is an FDA 510(k) premarket notification submitted by Oasis Medical, Inc. for the device "SOFT PLUG ABSORBABLE PLUG-SA". The FDA issued a decision of Substantially Equivalent on June 27, 2002. 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
June 27, 2002
Date Received
November 5, 2001
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