The following data is part of a premarket notification filed by Jas Diagnostics, Inc. with the FDA for Phosphorus Reagent.
| Device ID | K003912 |
| 510k Number | K003912 |
| Device Name: | PHOSPHORUS REAGENT |
| Classification | Phosphomolybdate (colorimetric), Inorganic Phosphorus |
| Applicant | JAS Diagnostics, Inc. 7220 NW 58TH ST. Miami, FL 33166 |
| Contact | David Johnston |
| Correspondent | David Johnston JAS Diagnostics, Inc. 7220 NW 58TH ST. Miami, FL 33166 |
| Product Code | CEO |
| CFR Regulation Number | 862.1580 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2000-12-19 |
| Decision Date | 2001-02-21 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00817274022481 | K003912 | 000 |
| 00817274022467 | K003912 | 000 |
| 00817274021910 | K003912 | 000 |
| 00817274021903 | K003912 | 000 |