510(k) K852013

GENTAMICIN KIT(FPIA) by Windsor Laboratories, Inc. — Product Code LCQ

K852013 is an FDA 510(k) premarket notification submitted by Windsor Laboratories, Inc. for the device "GENTAMICIN KIT(FPIA)". The FDA issued a decision of Substantially Equivalent on June 10, 1985. The device falls under product code LCQ (Fluorescent Immunoassay Gentamicin), a Class II device regulated under 21 CFR 862.3450. Windsor Laboratories, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 10, 1985
Date Received
May 9, 1985
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Fluorescent Immunoassay Gentamicin
Device Class
Class II
Regulation Number
862.3450
Review Panel
TX
Submission Type