510(k) K935226

I/V POLE by Optical Micro Systems, Inc. — Product Code KYG

K935226 is an FDA 510(k) premarket notification submitted by Optical Micro Systems, Inc. for the device "I/V POLE". The FDA issued a decision of Substantially Equivalent on February 16, 1994. The device falls under product code KYG (Device, Irrigation, Ocular Surgery), a Class I device regulated under 21 CFR 886.4360. Optical Micro Systems, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 16, 1994
Date Received
November 1, 1993
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