ESTRONE ANALYSIS PRODUCTS RADIOIMMUNOASSAY ESTRONE
FDA 510(k) clearance K864966 · decided 1987-01-09
Clearance details
- K-number
- K864966
- Device name
- ESTRONE ANALYSIS PRODUCTS RADIOIMMUNOASSAY ESTRONE
- Applicant
- Diagnostics Biochem Canada, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1986-12-22
- Decision date
- 1987-01-09
- Days to decision
- 18 days
- Clearance type
- Traditional
- Product code
- CGF
- Device class
- 1
- Regulation number
- 862.1280
- Medical specialty
- Clinical Chemistry
- Advisory committee
- Clinical Chemistry
- Location
- London, Ontario, CA
- 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 |
|---|---|---|
| DSL ESTRONE-SULFATE RIA (K970915) | Diagnostic Systems Laboratories, Inc. | 1997-05-16 |
| DSL ESTRONE (DSL 8700) (K935013) | Diagnostic Systems Laboratories, Inc. | 1994-06-16 |
| IMMOPHASE D-TE 3 RADIOIMMUNOASSAY (K833406) | Corning Medical & Scientific | 1984-01-24 |
Recalls involving this device
No recalls on record reference this clearance.