510(k) K820187
- Device
- Syva Advance Sys. Emit,(r)-aed(r) Pheny
- Applicant
- SYVA CO.
- 510(k) number
- K820187
- Product code
- LES
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1982-02-12
- Date received
- 1982-01-25
- Regulation
- 862.3350
- Classification name
- Fluorescent Immunoassay, Diphenylhydantoin
- 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
Source Documents#
510(k) summary PDF not indicated by FDA
Other 510(k) Records For Product Code LES#
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K865102 | IMMPULSE COATED TUBE PHENYTOIN ASSAY REAGENTS | Sclavo, Inc. | 1987-01-13 |
| K844990 | SYVA ADVANCE EMIT PHENYTOIN ASSAY | Syva Co. | 1985-01-23 |
| K831154 | STRATUS PHENYTOIN FLUOROMETRIC ENZYME | American Dade | 1983-05-16 |
| K813538 | PHENYTOIN FLUORESCENT IMMUNOASSAY | American Diagnostic Corp. | 1981-12-31 |
| K811025 | AMES TDA TM PHENYTOIN TEST | Miles Laboratories, Inc. | 1981-04-29 |
| K801736 | AMES TDA TM PHENYTOIN TEST | Miles Laboratories, Inc. | 1980-08-20 |