510(k) K862209

ALT (SGPT) REAGENT SET (UV RATE) by Sterling Diagnostics, Inc. — Product Code CKA

K862209 is an FDA 510(k) premarket notification submitted by Sterling Diagnostics, Inc. for the device "ALT (SGPT) REAGENT SET (UV RATE)". The FDA issued a decision of Substantially Equivalent on June 25, 1986. The device falls under product code CKA (Nadh Oxidation/Nad Reduction, Alt/Sgpt), a Class I device regulated under 21 CFR 862.1030. Sterling Diagnostics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 25, 1986
Date Received
June 10, 1986
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Nadh Oxidation/Nad Reduction, Alt/Sgpt
Device Class
Class I
Regulation Number
862.1030
Review Panel
CH
Submission Type