510(k) K812077
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