510(k) K890027

QUIKREAD CHEM. ANALYZER & CHOLES. FOR WHOLE BLOOD by Photec Diagnostics, Inc. — Product Code CHH

K890027 is an FDA 510(k) premarket notification submitted by Photec Diagnostics, Inc. for the device "QUIKREAD CHEM. ANALYZER & CHOLES. FOR WHOLE BLOOD". The FDA issued a decision of Substantially Equivalent on April 26, 1989. The device falls under product code CHH (Enzymatic Esterase--Oxidase, Cholesterol), a Class I device regulated under 21 CFR 862.1175. Photec Diagnostics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 26, 1989
Date Received
January 4, 1989
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Enzymatic Esterase--Oxidase, Cholesterol
Device Class
Class I
Regulation Number
862.1175
Review Panel
CH
Submission Type