510(k) K001123

KURZ UPPER EYELID IMPLANT SIZERS, MODEL 8000 111 by Heinz Kurz GmbH Medizintechnik — Product Code MML

K001123 is an FDA 510(k) premarket notification submitted by Heinz Kurz GmbH Medizintechnik for the device "KURZ UPPER EYELID IMPLANT SIZERS, MODEL 8000 111". The FDA issued a decision of Substantially Equivalent on April 21, 2000. The device falls under product code MML (Weights, Eyelid, External), a Class II device regulated under 21 CFR 886.5700. Heinz Kurz GmbH Medizintechnik has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 21, 2000
Date Received
April 7, 2000
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)