510(k) K854873

INTRAOCULAR PRESSURE REDUCER by Mira, Inc. — Product Code LCR

K854873 is an FDA 510(k) premarket notification submitted by Mira, Inc. for the device "INTRAOCULAR PRESSURE REDUCER". The FDA issued a decision of Substantially Equivalent on February 4, 1986. The device falls under product code LCR (Fluorescent Immunoassay, Tobramycin), a Class II device regulated under 21 CFR 862.3900. Mira, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 4, 1986
Date Received
December 4, 1985
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Fluorescent Immunoassay, Tobramycin
Device Class
Class II
Regulation Number
862.3900
Review Panel
TX
Submission Type