510(k) K854392

TOBRAMYCIN KIT(FPIA)FLUORESCENCE POLARIZATION IMMU by Windsor Laboratories, Inc. — Product Code LFW

K854392 is an FDA 510(k) premarket notification submitted by Windsor Laboratories, Inc. for the device "TOBRAMYCIN KIT(FPIA)FLUORESCENCE POLARIZATION IMMU". The FDA issued a decision of Substantially Equivalent on December 5, 1985. The device falls under product code LFW (Fluorescence Polarization Immunoassay, Tobramycin), a Class II device regulated under 21 CFR 862.3900. Windsor Laboratories, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 5, 1985
Date Received
October 31, 1985
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

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