510(k) K852343
- Device
- Dig Radioimmunoassay Test System
- Applicant
- M NOBIRD, INC.
- 510(k) number
- K852343
- Product code
- DNL
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1985-07-09
- Date received
- 1985-06-03
- Regulation
- 862.3320
- Classification name
- Radioimmunoassay, Digoxin (125-I), Rabbit Antibody, Second Antibody Sep.
- Medical specialty
- Clinical Toxicology
- Review panel
- Clinical Toxicology
- Device class
- 2
- Clearance type
- Traditional
- Third party reviewed
- No
Applicant Contact#
- Contact
- MICHAEL R FALVO
- Address
- 729 W. 16th St., C-4 Costa Mesa CA US 92627 92627
Source Documents#
510(k) summary PDF not indicated by FDA
Other 510(k) Records For Product Code DNL#
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K852291 | TIPSEP DIGOXIN RIA | Nuclear Diagnostics, Inc. | 1985-06-25 |
| K811212 | DIGOXIN (RIA) KIT | Immuno Assay Corp. | 1981-05-21 |
| K810966 | DIAGOXIN SQUIBB RADIOIMMUNOASSAY KIT | E. R. Squibb & Sons, Inc. | 1981-04-21 |
| K802841 | DIGOXIN RADIOIMMUNOASSAY KIT | American Diagnostic Corp. | 1980-12-18 |
| K781495 | RIANEN ASSAY SYSTEM, 125I KIT | New England Nuclear | 1978-09-14 |
| K772110 | IN VITRO DIGOXIN RIA TEST | Clinical Assays, Inc. | 1977-11-22 |