510(k) K010353

MED-LOGICS DISPOSABLE ALK TUBING by Med-Logics, Inc. — Product Code KYG

K010353 is an FDA 510(k) premarket notification submitted by Med-Logics, Inc. for the device "MED-LOGICS DISPOSABLE ALK TUBING". The FDA issued a decision of Substantially Equivalent on April 27, 2001. The device falls under product code KYG (Device, Irrigation, Ocular Surgery), a Class I device regulated under 21 CFR 886.4360. Med-Logics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 27, 2001
Date Received
February 6, 2001
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Device, Irrigation, Ocular Surgery
Device Class
Class I
Regulation Number
886.4360
Review Panel
OP
Submission Type