510(k) K860477

URIC ACID REAGNET SET (TRINDER) by Sterling Diagnostics, Inc. — Product Code KNK

K860477 is an FDA 510(k) premarket notification submitted by Sterling Diagnostics, Inc. for the device "URIC ACID REAGNET SET (TRINDER)". The FDA issued a decision of Substantially Equivalent on April 3, 1986. The device falls under product code KNK (Acid, Uric, Uricase (Colorimetric)), a Class I device regulated under 21 CFR 862.1775. Sterling Diagnostics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 3, 1986
Date Received
February 7, 1986
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