ALIZARIN SULFONATE, CALCIUM
FDA 510(k) clearance K801290 · decided 1980-06-30
Clearance details
- K-number
- K801290
- Device name
- ALIZARIN SULFONATE, CALCIUM
- Applicant
- Union Carbide Corp.
- Decision
- Substantially Equivalent
- Date received
- 1980-05-30
- Decision date
- 1980-06-30
- Days to decision
- 31 days
- Clearance type
- Traditional
- Product code
- CID
- Device class
- 2
- Regulation number
- 862.1145
- Medical specialty
- Clinical Chemistry
- Advisory committee
- Clinical Chemistry
- 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 |
|---|---|---|
| KODAK EKTACHEM DT SLIDES (CA) (K870035) | Eastman Kodak Company | 1987-05-12 |
Recalls involving this device
No recalls on record reference this clearance.