510(k) K970560

URIC ACID (LIQUID) REAGENT SET by Pointe Scientific, Inc., — Product Code KNK

K970560 is an FDA 510(k) premarket notification submitted by Pointe Scientific, Inc., for the device "URIC ACID (LIQUID) REAGENT SET". The FDA issued a decision of Substantially Equivalent on March 11, 1997. The device falls under product code KNK (Acid, Uric, Uricase (Colorimetric)), a Class I device regulated under 21 CFR 862.1775. Pointe Scientific, Inc., has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 11, 1997
Date Received
February 13, 1997
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