510(k) K860475

HEMOGLOBIN REAGENT SET by Sterling Diagnostics, Inc. — Product Code KHG

K860475 is an FDA 510(k) premarket notification submitted by Sterling Diagnostics, Inc. for the device "HEMOGLOBIN REAGENT SET". The FDA issued a decision of Substantially Equivalent on March 3, 1986. The device falls under product code KHG (Whole Blood Hemoglobin Determination), a Class II device regulated under 21 CFR 864.7500. Sterling Diagnostics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 3, 1986
Date Received
February 7, 1986
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