510(k) K872653

EASY-TEST HEMOGLOBIN (HGB) ITEM #16685 by Em Diagnostic Systems, Inc. — Product Code KHG

K872653 is an FDA 510(k) premarket notification submitted by Em Diagnostic Systems, Inc. for the device "EASY-TEST HEMOGLOBIN (HGB) ITEM #16685". The FDA issued a decision of Substantially Equivalent on July 23, 1987. The device falls under product code KHG (Whole Blood Hemoglobin Determination), a Class II device regulated under 21 CFR 864.7500. Em Diagnostic Systems, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 23, 1987
Date Received
July 7, 1987
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Whole Blood Hemoglobin Determination
Device Class
Class II
Regulation Number
864.7500
Review Panel
HE
Submission Type