The following data is part of a premarket notification filed by American Monitor Corp. with the FDA for Phosphorus.
Device ID | K895999 |
510k Number | K895999 |
Device Name: | PHOSPHORUS |
Classification | Phosphomolybdate (colorimetric), Inorganic Phosphorus |
Applicant | AMERICAN MONITOR CORP. P.O. BOX 68505 Indianapolis, IN 46268 |
Contact | Jennifer Line |
Correspondent | Jennifer Line AMERICAN MONITOR CORP. P.O. BOX 68505 Indianapolis, IN 46268 |
Product Code | CEO |
CFR Regulation Number | 862.1580 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1989-10-13 |
Decision Date | 1990-01-11 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
PHOSPHORUS 90623821 not registered Live/Pending |
Phosphorus Cybersecurity Inc. 2021-04-05 |
PHOSPHORUS 87083408 5215288 Live/Registered |
PHOSPHORUS, INC. 2016-06-24 |
PHOSPHORUS 85479035 not registered Dead/Abandoned |
White Oak Technologies, Inc. 2011-11-22 |