510(k) K953581

FIRST RESPONSE OVULATION PREDICTOR TEST by Armkel, LLC — Product Code CEP

K953581 is an FDA 510(k) premarket notification submitted by Armkel, LLC for the device "FIRST RESPONSE OVULATION PREDICTOR TEST". The FDA issued a decision of Substantially Equivalent on October 3, 1995. The device falls under product code CEP (Radioimmunoassay, Luteinizing Hormone), a Class I device regulated under 21 CFR 862.1485. Armkel, LLC has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 3, 1995
Date Received
August 1, 1995
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Radioimmunoassay, Luteinizing Hormone
Device Class
Class I
Regulation Number
862.1485
Review Panel
CH
Submission Type