510(k) K951071

ALKO SLOPE THB SOLUTION FOR CORNING 280, 288 AND 2500 ANALYZERS by Alko Diagnostic Corp. — Product Code KRZ

K951071 is an FDA 510(k) premarket notification submitted by Alko Diagnostic Corp. for the device "ALKO SLOPE THB SOLUTION FOR CORNING 280, 288 AND 2500 ANALYZERS". The FDA issued a decision of Substantially Equivalent on July 24, 1995. The device falls under product code KRZ (Calibrator For Hemoglobin And Hematocrit Measurement), a Class II device regulated under 21 CFR 864.8165. Alko Diagnostic Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 24, 1995
Date Received
March 8, 1995
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Calibrator For Hemoglobin And Hematocrit Measurement
Device Class
Class II
Regulation Number
864.8165
Review Panel
HE
Submission Type