510(k) K910431

HEMOCARD CONTROL by Isolab, Inc. — Product Code JCM

K910431 is an FDA 510(k) premarket notification submitted by Isolab, Inc. for the device "HEMOCARD CONTROL". The FDA issued a decision of Substantially Equivalent on March 11, 1991. 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
March 11, 1991
Date Received
February 1, 1991
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