510(k) K894122

LEECO VIS-DISK STREP-A (EIA) by Leeco Diagnostics, Inc. — Product Code GTZ

K894122 is an FDA 510(k) premarket notification submitted by Leeco Diagnostics, Inc. for the device "LEECO VIS-DISK STREP-A (EIA)". The FDA issued a decision of Substantially Equivalent on August 15, 1989. The device falls under product code GTZ (Antisera, All Groups, Streptococcus Spp.), a Class I device regulated under 21 CFR 866.3740. Leeco Diagnostics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 15, 1989
Date Received
June 12, 1989
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Antisera, All Groups, Streptococcus Spp.
Device Class
Class I
Regulation Number
866.3740
Review Panel
MI
Submission Type