K173123 is an FDA 510(k) clearance for the Pulse Oximeter. This device is classified as a Oximeter (Class II - Special Controls, product code DQA).
Submitted by Shenzhen Imdk Medical Technology Co., Ltd. (Guangming District, Shenzhen, CN). The FDA issued a Cleared decision on August 13, 2018, 318 days after receiving the submission on September 29, 2017.
This device falls under the Anesthesiology FDA review panel. Regulated under 21 CFR 870.2700.
| 510(k) Number | K173123 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | September 29, 2017 |
| Decision Date | August 13, 2018 |
| Days to Decision | 318 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 |