(125 I) DIGITOXIN RIA KIT
FDA 510(k) clearance K780766 · decided 1978-07-27
Clearance details
- K-number
- K780766
- Device name
- (125 I) DIGITOXIN RIA KIT
- Applicant
- Diagnostic Products Corp.
- Decision
- Substantially Equivalent
- Date received
- 1978-05-05
- Decision date
- 1978-07-27
- Days to decision
- 83 days
- Clearance type
- Traditional
- Product code
- LCW
- Device class
- 2
- Regulation number
- 862.3300
- Medical specialty
- Clinical Toxicology
- Advisory committee
- Clinical Toxicology
- Location
- Mchenry, IL, US
- Third-party review
- No
- Expedited review
- No
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Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
| Record | Firm | Date |
|---|---|---|
| MATCHED COMPONENT SET FOR DIGITOXIN (K834080) | Cambridge Medical Technology | 1984-02-04 |
| ENDAB DIGITOXIN ENZYME IMMUNOASSAY KIT (K802461) | Immunotech Corp. | 1980-10-31 |
Recalls involving this device
No recalls on record reference this clearance.