510(k) K831814

CALIBRATION STANDARD-HEMOGLOBIN by United Diagnostics, Inc. — Product Code KRZ

K831814 is an FDA 510(k) premarket notification submitted by United Diagnostics, Inc. for the device "CALIBRATION STANDARD-HEMOGLOBIN". The FDA issued a decision of Substantially Equivalent on July 28, 1983. The device falls under product code KRZ (Calibrator For Hemoglobin And Hematocrit Measurement), a Class II device regulated under 21 CFR 864.8165. United Diagnostics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 28, 1983
Date Received
June 6, 1983
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