Ria Test Kit, Centria Digoxin
FDA 510(k) K790540 · Ventrex Laboratories, Inc.
510(k) numberK790540
Submission
- Device name
- Ria Test Kit, Centria Digoxin
- Applicant
- Ventrex Laboratories, Inc.
Walker, MI, US - Received
- March 20, 1979
- Decision date
- April 23, 1979
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- DPB – Radioimmunoassay, Digoxin (125-I), Rabbit Antibody, Charcoal Sep.
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 862.3320
- Specialty
- Clinical Toxicology
Other 510(k)s with product code DPB
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K853021 | Optimate Digoxin TestDPB · Traditional | Miles Laboratories, Inc. | 08/07/1985SE |
| K823014 | Digoxin KitDPB · Traditional | Pcl-Ria, Inc. | 11/01/1982SE |
| K821811 | 125I Digoxin Radioimmunoassay KitDPB · Traditional | Cambridge Medical Technology | 07/02/1982SE |
| K820274 | Digoxin RadioimmunoassayDPB · Traditional | American Diagnostic Corp. | 02/23/1982SE |
| K792153 | Digoxin Radioimmunoassay SystemDPB · Traditional | Radioimmunoassay, Inc. | 11/13/1979SE |
| K790602 | Ria, DIGNXIN-125-IDPB · Traditional | Endocrine-Metabolic Center | 07/30/1979SE |
| K772306 | 125I Digoxin Test SetDPB · Traditional | Wien Laboratories, Inc. | 12/22/1977SE |
| K771525 | 125 I Digoxin Ria KitDPB · Traditional | Diagnostic Products Corp. | 10/14/1977SE |
| K760883 | Digi-Tab-Ria Digoxin RadiommunoassayDPB · Traditional | Nuclear Medical Laboratories, Inc. | 11/19/1976SE |
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| K913434 | Ventrex Coated Tube Intact PTHCEW · Traditional | 10/25/1991SE |
| K905612 | Ventrex Coated Tube Ige RadioimmunoassayDGC · Traditional | 02/21/1991SE |
| K905636 | Ventrex Coated Tube Ige Enzyme ImmunoassayDHB · Traditional | 02/07/1991SE |
| K905247 | SHBG Irma KitCDZ · Traditional | 01/17/1991SE |
| K904330 | Turbo-Rast Specific Ige AssayDHB · Traditional | 12/07/1990SE |
| K903000 | Turbo-Rast Specific Ige AssayJHR · Traditional | 07/31/1990SE |
| K897083 | Ventresign Strep a TestGTZ · Traditional | 01/22/1990SE |
| K895649 | Coated Tube High Sensitivity TSH 200 Uiu/Ml Stan.JIT · Traditional | 01/18/1990SE |
Questions and answers
When was Ria Test Kit, Centria Digoxin cleared by the FDA?
Ria Test Kit, Centria Digoxin (K790540) received a 510(k) decision of Substantially Equivalent on April 23, 1979, 34 days after the submission was received.
What is the product code of K790540?
The FDA product code is DPB – Radioimmunoassay, Digoxin (125-I), Rabbit Antibody, Charcoal Sep., a Class II (moderate risk) device regulated under 21 CFR 862.3320.