510(k) K821658

HEMOGLOBIN REAGENT by Anco Medical Reagents & Assoc. — Product Code KHG

K821658 is an FDA 510(k) premarket notification submitted by Anco Medical Reagents & Assoc. for the device "HEMOGLOBIN REAGENT". The FDA issued a decision of Substantially Equivalent on June 25, 1982. The device falls under product code KHG (Whole Blood Hemoglobin Determination), a Class II device regulated under 21 CFR 864.7500. Anco Medical Reagents & Assoc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 25, 1982
Date Received
June 4, 1982
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