510(k) K012038

JAS URIC ACID LIQUID REAGENT by Jas Diagnostics, Inc. — Product Code KNK

K012038 is an FDA 510(k) premarket notification submitted by Jas Diagnostics, Inc. for the device "JAS URIC ACID LIQUID REAGENT". The FDA issued a decision of Substantially Equivalent on August 21, 2001. The device falls under product code KNK (Acid, Uric, Uricase (Colorimetric)), a Class I device regulated under 21 CFR 862.1775. Jas Diagnostics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 21, 2001
Date Received
June 29, 2001
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Acid, Uric, Uricase (Colorimetric)
Device Class
Class I
Regulation Number
862.1775
Review Panel
CH
Submission Type