K122060 is an FDA 510(k) clearance for the CLEVER TD-7001NEBULIZER. This device is classified as a Nebulizer (direct Patient Interface) (Class II - Special Controls, product code CAF).
Submitted by Taidoc Technology Corporation (New Taipei City, TW). The FDA issued a Cleared decision on March 21, 2013, 251 days after receiving the submission on July 13, 2012.
This device falls under the Anesthesiology FDA review panel. Regulated under 21 CFR 868.5630.
| 510(k) Number | K122060 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | July 13, 2012 |
| Decision Date | March 21, 2013 |
| Days to Decision | 251 days |
| Submission Type | Traditional |
| Review Panel | Anesthesiology (AN) |
| Summary | Summary PDF |
| Product Code | CAF — Nebulizer (direct Patient Interface) |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 868.5630 |