510(k) K823741
- Device
- Advance Emit-aed Primedone Assay
- Applicant
- SYVA CO.
- 510(k) number
- K823741
- Product code
- LFT
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1983-01-07
- Date received
- 1982-12-13
- Regulation
- 862.3680
- Classification name
- Fluorescent Immunoassay, Primidone
- Medical specialty
- Clinical Toxicology
- Review panel
- Clinical Toxicology
- Device class
- 2
- Clearance type
- Traditional
- Third party reviewed
- No
Applicant Contact#
- Address
- 803 N. Front St. Suite 3 Mchenry IL US 60050 60050
FDA Registration Numbers#
- 9610126
Source Documents#
510(k) summary PDF not indicated by FDA
Other 510(k) Records For Product Code LFT#
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K950028 | PRIMIDONE FPIA REAGENT SET AND CALIBRATORS | Sigma Diagnostics, Inc. | 1995-03-21 |
| K904683 | STRATUS PRIMIDONE FLUOROMETRIC ENZYME | Baxter Healthcare Corp | 1990-11-28 |
| K895567 | PRIMIDONE (FPIA) KIT | Tudor Laboratories, Inc. | 1989-10-20 |
| K852318 | COBAS FP REAGEN FOR PRIMIDONE & PRIMI CALIBRATORS | Roche Diagnostic Systems, Inc. | 1985-06-25 |
| K842196 | STRATUS PRIMIDONE FLOROMETRIC ENZY | American Dade | 1984-07-11 |
| K822229 | PRIMIDONE FLUORESCENT IMMUNOASSAY | American Diagnostic Corp. | 1982-08-12 |
| K811007 | AMES TDA TM PRIMIDONE TEST | Miles Laboratories, Inc. | 1981-04-29 |