K151024 is an FDA 510(k) clearance for the Finger Type Pulse Oximeter. This device is classified as a Oximeter (Class II - Special Controls, product code DQA).
Submitted by Taidoc Technology Corporation (New Taipei City, TW). The FDA issued a Cleared decision on March 2, 2016, 321 days after receiving the submission on April 16, 2015.
This device falls under the Anesthesiology FDA review panel. Regulated under 21 CFR 870.2700.
| 510(k) Number | K151024 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | April 16, 2015 |
| Decision Date | March 02, 2016 |
| Days to Decision | 321 days |
| Submission Type | Traditional |
| Review Panel | Anesthesiology (AN) |
| Summary | Summary PDF |
| Product Code | DQA — Oximeter |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 870.2700 |