510(k) K033293

MED-LOGICS, MODEL ML7090 by Med-Logics, Inc. — Product Code HNO

K033293 is an FDA 510(k) premarket notification submitted by Med-Logics, Inc. for the device "MED-LOGICS, MODEL ML7090". The FDA issued a decision of Substantially Equivalent on January 13, 2004. The device falls under product code HNO (Keratome, Ac-Powered), a Class I device regulated under 21 CFR 886.4370. Med-Logics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 13, 2004
Date Received
October 14, 2003
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Keratome, Ac-Powered
Device Class
Class I
Regulation Number
886.4370
Review Panel
OP
Submission Type