510(k) K897190

LOOK TEMPORARY INTRACANALICULAR COLLAGEN IMPLANT by Look, Inc. — Product Code LZU

K897190 is an FDA 510(k) premarket notification submitted by Look, Inc. for the device "LOOK TEMPORARY INTRACANALICULAR COLLAGEN IMPLANT". The FDA issued a decision of Substantially Equivalent on March 28, 1990. The device falls under product code LZU (Plug, Punctum), a Class U device. Look, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 28, 1990
Date Received
December 28, 1989
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