510(k) K822327

CALIBRATOR FOR HEMOGLOBIN & HEMOCRIT by Interscience, Inc. — Product Code KRZ

K822327 is an FDA 510(k) premarket notification submitted by Interscience, Inc. for the device "CALIBRATOR FOR HEMOGLOBIN & HEMOCRIT". The FDA issued a decision of Substantially Equivalent on November 16, 1982. The device falls under product code KRZ (Calibrator For Hemoglobin And Hematocrit Measurement), a Class II device regulated under 21 CFR 864.8165. Interscience, Inc. has at least 3 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 16, 1982
Date Received
August 3, 1982
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