DIGOXIN RIA (PEG) KIT
FDA 510(k) clearance K781335 · decided 1978-08-31
Clearance details
- K-number
- K781335
- Device name
- DIGOXIN RIA (PEG) KIT
- Applicant
- Ortho Diagnostics, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1978-08-02
- Decision date
- 1978-08-31
- Days to decision
- 29 days
- Clearance type
- Traditional
- Product code
- DOG
- Device class
- 2
- Regulation number
- 862.3320
- 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 |
|---|---|---|
| DCA DIGOX-SYN RIA TEST (K810477) | Diagnostic Corp. of America | 1981-03-11 |
| IMMU-TRACE DIGOXIN (125I) RADIOIMMUN. (K803045) | American Dade | 1980-12-22 |
| EMIT DIGOKIN ASSAY (K760709) | Syva Co. | 1976-10-21 |
| DATA-TOPE SYSTEM DIGOXIN RIA (K760416) | Dade, Baxter Travenol Diagnostics, Inc. | 1976-08-23 |
Recalls involving this device
No recalls on record reference this clearance.