510(k) K893912

TECHNICON RA SYSTEMS GENTAMICIN TEST METHOD by Technicon Instruments Corp. — Product Code LCD

K893912 is an FDA 510(k) premarket notification submitted by Technicon Instruments Corp. for the device "TECHNICON RA SYSTEMS GENTAMICIN TEST METHOD". The FDA issued a decision of Substantially Equivalent on August 21, 1989. The device falls under product code LCD (Enzyme Immunoassay, Gentamicin), a Class II device regulated under 21 CFR 862.3450. Technicon Instruments Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 21, 1989
Date Received
May 30, 1989
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

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