FDA product code CID: Alizarin Sulfonate, Calcium
CID is the FDA product code for alizarin sulfonate, calcium. It is a Class II device, regulated under 21 CFR 862.1145 and reviewed by the Clinical Chemistry panel. FDA has cleared 2 510(k) submissions under CID, from 2 different applicants. The average 510(k) review took 79 days (median 79).
Classification
| Field | Value |
|---|---|
| Device name | Alizarin Sulfonate, Calcium |
| Device class | Class II |
| Regulation | 21 CFR 862.1145 |
| Review panel | CH — Clinical Chemistry |
| Medical specialty | Clinical Chemistry |
| Premarket route | 510(k) |
| Third-party 510(k) review eligible | Yes |
Compare with all 510(k) review times · Search every CID clearance
Top CID applicants
| Applicant | Clearances | Latest |
|---|---|---|
| Eastman Kodak Company | 1 | 1987-05-12 |
| Union Carbide Corp. | 1 | 1980-06-30 |
Most recent CID clearances
| 510(k) | Applicant | Device | Decision date | Review days |
|---|---|---|---|---|
| K870035 | Eastman Kodak Company | KODAK EKTACHEM DT SLIDES (CA) | 1987-05-12 | 127 |
| K801290 | Union Carbide Corp. | ALIZARIN SULFONATE, CALCIUM | 1980-06-30 | 31 |
Recalls for CID devices
openFDA lists no recalls for product code CID.
Frequently asked questions
What is FDA product code CID?
CID is the FDA product code for alizarin sulfonate, calcium. It is a Class II device, regulated under 21 CFR 862.1145 and reviewed by the Clinical Chemistry panel.
What device class is CID?
Class II, regulation 21 CFR 862.1145. Typical premarket route: 510(k).
How long does a 510(k) take for product code CID?
Across 2 cleared submissions the average was 79 days from receipt to decision (median 79).
Which companies have the most CID clearances?
Eastman Kodak Company (1); Union Carbide Corp. (1).
Next steps
- Run an FDA pathway report with predicate devices for product code CID
- Run a recall and safety report across every CID manufacturer
- Watch product code CID for new clearances and recalls
Source: openFDA device classification, 510(k), PMA, De Novo and recall data (public domain). Review days run from FDA receipt to decision. Not regulatory advice.
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