The following data is part of a premarket notification filed by Nms Pharmaceuticals, Inc. with the FDA for Foretel, Color Ovulation Test.
Device ID | K860828 |
510k Number | K860828 |
Device Name: | FORETEL, COLOR OVULATION TEST |
Classification | Radioimmunoassay, Luteinizing Hormone |
Applicant | NMS PHARMACEUTICALS, INC. 1533 MONROVIA AVE. Newport Beach, CA 92663 |
Contact | Perry G Rucker |
Correspondent | Perry G Rucker NMS PHARMACEUTICALS, INC. 1533 MONROVIA AVE. Newport Beach, CA 92663 |
Product Code | CEP |
CFR Regulation Number | 862.1485 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1986-03-05 |
Decision Date | 1986-08-04 |