510(k) K911613

VAR AURAL GROM AG/S9,SD8.00.28.5/0.2 NS/S/6823 1.4 by Exmoor Plastics , Ltd. — Product Code LCR

K911613 is an FDA 510(k) premarket notification submitted by Exmoor Plastics , Ltd. for the device "VAR AURAL GROM AG/S9,SD8.00.28.5/0.2 NS/S/6823 1.4". The FDA issued a decision of Substantially Equivalent on June 28, 1991. The device falls under product code LCR (Fluorescent Immunoassay, Tobramycin), a Class II device regulated under 21 CFR 862.3900. Exmoor Plastics , Ltd. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 28, 1991
Date Received
April 3, 1991
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