510(k) K812077

HELENA SICKLE-THAL QUIK COLUMN METHOD by Helena Laboratories — Product Code JPD

K812077 is an FDA 510(k) premarket notification submitted by Helena Laboratories for the device "HELENA SICKLE-THAL QUIK COLUMN METHOD". The FDA issued a decision of Substantially Equivalent on August 18, 1981. The device falls under product code JPD (Hemoglobin A2 Quantitation), a Class II device regulated under 21 CFR 864.7400. Helena Laboratories has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 18, 1981
Date Received
July 22, 1981
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Hemoglobin A2 Quantitation
Device Class
Class II
Regulation Number
864.7400
Review Panel
HE
Submission Type