510(k) K844322
- Device
- SGOT REAGENT SET
- Applicant
- LIVONIA DIAGNOSTICS, INC.
- 510(k) number
- K844322
- Product code
- CIQ
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1984-11-27
- Date received
- 1984-11-07
- Regulation
- 862.1100
- Classification name
- Diazo, Ast/sgot
- Medical specialty
- Clinical Chemistry
- Review panel
- Clinical Chemistry
- Device class
- 2
- Clearance type
- Traditional
- Third party reviewed
- No
Applicant Contact#
- Contact
- WALTER H LAMBERT
- Address
- 33041 W. Eight Mile Rd. Livonia MI US 48152 48152
FDA Registration Numbers#
- 1832216
Source Documents#
510(k) summary PDF not indicated by FDA
Other 510(k) Records For Product Code CIQ #
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K881173 | ASPARTATE AMINOTRANSFERASE (COLORIMETRIC METHOD) | Tech-Co, Inc. | 1988-06-07 |
| K860216 | SGOT (AST) REAGENT SET | Sterling Diagnostics, Inc. | 1986-04-03 |
| K855189 | GLUTAMIC OXALOACETIC TRANSAMINASE REAGENT SET | Technostics Intl. | 1986-01-14 |
| K841065 | SGOT REAGENT SET | Medical Specialties, Inc. | 1984-05-01 |
| K821209 | SGOT REAGENT SET | Omega Medical Electronics | 1982-07-14 |
| K820466 | SGOT REAGENT SET | Anco Medical Reagents & Assoc. | 1982-03-11 |
Legacy Summary#
Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links Follow FDA En Español Home Food Drugs Medical Devices Radiation-Emitting Products Vaccines, Blood & Biologics Animal & Veterinary Cosmetics Tobacco Products FDA Home Medical Devices Databases
FDA Review#
Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links Follow FDA En Español Home Food Drugs Medical Devices Radiation-Emitting Products Vaccines, Blood & Biologics Animal & Veterinary Cosmetics Tobacco Products FDA Home Medical Devices Databases