The following data is part of a premarket notification filed by American Dade with the FDA for Paraamax Chloride Determination By Ise.
Device ID | K854651 |
510k Number | K854651 |
Device Name: | PARAAMAX CHLORIDE DETERMINATION BY ISE |
Classification | Radioimmunoassay, Follicle-stimulating Hormone |
Applicant | AMERICAN DADE P.O. BOX 25101 Santa Ana, CA 92799 |
Contact | James Keller |
Correspondent | James Keller AMERICAN DADE P.O. BOX 25101 Santa Ana, CA 92799 |
Product Code | CGJ |
CFR Regulation Number | 862.1300 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1985-11-19 |
Decision Date | 1985-12-13 |