The following data is part of a premarket notification filed by Biotrol, Usa, Inc. with the FDA for Biotrol Magnesium Calmagite.
Device ID | K873180 |
510k Number | K873180 |
Device Name: | BIOTROL MAGNESIUM CALMAGITE |
Classification | Photometric Method, Magnesium |
Applicant | BIOTROL, USA, INC. P.O. BOX 562 Berwyn, PA 19312 |
Contact | Allan C Murphy |
Correspondent | Allan C Murphy BIOTROL, USA, INC. P.O. BOX 562 Berwyn, PA 19312 |
Product Code | JGJ |
CFR Regulation Number | 862.1495 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1987-08-12 |
Decision Date | 1987-09-02 |