510(k) K941220

DUPONT ACA PLUS PROLACTIN (PROL) METHOD by Dupont Medical Products — Product Code CFT

K941220 is an FDA 510(k) premarket notification submitted by Dupont Medical Products for the device "DUPONT ACA PLUS PROLACTIN (PROL) METHOD". The FDA issued a decision of Substantially Equivalent on June 3, 1994. The device falls under product code CFT (Radioimmunoassay, Prolactin (Lactogen)), a Class I device regulated under 21 CFR 862.1625. Dupont Medical Products has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 3, 1994
Date Received
March 14, 1994
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Radioimmunoassay, Prolactin (Lactogen)
Device Class
Class I
Regulation Number
862.1625
Review Panel
CH
Submission Type