510(k) K924173

HEMOCARD(TM) CONTROL by Isolab, Inc. — Product Code JCM

K924173 is an FDA 510(k) premarket notification submitted by Isolab, Inc. for the device "HEMOCARD(TM) CONTROL". The FDA issued a decision of Substantially Equivalent on December 1, 1992. The device falls under product code JCM (Control, Hemoglobin, Abnormal), a Class II device regulated under 21 CFR 864.7415. Isolab, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 1, 1992
Date Received
August 19, 1992
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Control, Hemoglobin, Abnormal
Device Class
Class II
Regulation Number
864.7415
Review Panel
HE
Submission Type