510(k) K870363

HAEMOGLOBIN REAGENT - CYANMETHAEMOGLOBIN METHOD by Trace Scientific , Ltd. — Product Code KHG

K870363 is an FDA 510(k) premarket notification submitted by Trace Scientific , Ltd. for the device "HAEMOGLOBIN REAGENT - CYANMETHAEMOGLOBIN METHOD". The FDA issued a decision of Substantially Equivalent on March 16, 1987. The device falls under product code KHG (Whole Blood Hemoglobin Determination), a Class II device regulated under 21 CFR 864.7500. Trace Scientific , Ltd. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 16, 1987
Date Received
January 28, 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