The following data is part of a premarket notification filed by Em Diagnostic Systems, Inc. with the FDA for Emds Phosphorous (phos) Test.
Device ID | K935178 |
510k Number | K935178 |
Device Name: | EMDS PHOSPHOROUS (PHOS) TEST |
Classification | Phosphomolybdate (colorimetric), Inorganic Phosphorus |
Applicant | EM DIAGNOSTIC SYSTEMS, INC. DIV. OF EM INDUSTRIES INC. 480 DEMOCRAT RD. Gibbstown, NJ 08027 |
Contact | Carol Faulkner |
Correspondent | Carol Faulkner EM DIAGNOSTIC SYSTEMS, INC. DIV. OF EM INDUSTRIES INC. 480 DEMOCRAT RD. Gibbstown, NJ 08027 |
Product Code | CEO |
CFR Regulation Number | 862.1580 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1993-10-26 |
Decision Date | 1993-12-17 |