K860875 is an FDA 510(k) clearance for the CIRRUS DRUG NEBULIZER MK III. This device is classified as a Nebulizer, Medicinal, Non-ventilatory (atomizer) (Class I - General Controls, product code CCQ).
Submitted by Dhd Medical Products Div. Diemolding Corp. (Canastota, US). The FDA issued a Cleared decision on March 20, 1986, 23 days after receiving the submission on February 25, 1986.
This device falls under the Anesthesiology FDA review panel. Regulated under 21 CFR 868.5640.
| 510(k) Number | K860875 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | February 25, 1986 |
| Decision Date | March 20, 1986 |
| Days to Decision | 23 days |
| Submission Type | Traditional |
| Review Panel | Anesthesiology (AN) |
| Summary | — |
| Product Code | CCQ — Nebulizer, Medicinal, Non-ventilatory (atomizer) |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 868.5640 |