510(k) K994289

SUTUREGROOVE by Iop, Inc. — Product Code MML

K994289 is an FDA 510(k) premarket notification submitted by Iop, Inc. for the device "SUTUREGROOVE". The FDA issued a decision of Substantially Equivalent on April 17, 2000. The device falls under product code MML (Weights, Eyelid, External), a Class II device regulated under 21 CFR 886.5700. Iop, Inc. has at least 8 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 17, 2000
Date Received
December 21, 1999
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Weights, Eyelid, External
Device Class
Class II
Regulation Number
886.5700
Review Panel
OP
Submission Type

Gravity assisted treatment of lagophthalmos (incomplete eyelid closure)