510(k) K801290
- Device
- ALIZARIN SULFONATE, CALCIUM
- Applicant
- UNION CARBIDE CORP.
- 510(k) number
- K801290
- Product code
- CID
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1980-06-30
- Date received
- 1980-05-30
- Regulation
- 862.1145
- Classification name
- Alizarin Sulfonate, Calcium
- Medical specialty
- Clinical Chemistry
- Review panel
- Clinical Chemistry
- Device class
- 2
- Clearance type
- Traditional
- Third party reviewed
- No
Applicant Contact#
- Address
- 803 N. Front St. Suite 3 Mchenry IL US 60050 60050
Source Documents#
510(k) summary PDF not indicated by FDA
Other 510(k) Records For Product Code CID #
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K870035 | KODAK EKTACHEM DT SLIDES (CA) | Eastman Kodak Company | 1987-05-12 |
Legacy Summary#
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FDA Review#
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