K050169 is an FDA 510(k) clearance for the HL 200 ELECTRONIC STETHOSCOPE. This device is classified as a Stethoscope, Electronic (Class II - Special Controls, product code DQD).
Submitted by Health & Life Co., Ltd. (Flagstaff, US). The FDA issued a Cleared decision on April 5, 2005, 69 days after receiving the submission on January 26, 2005.
This device falls under the Cardiovascular FDA review panel. Regulated under 21 CFR 870.1875.
| 510(k) Number | K050169 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | January 26, 2005 |
| Decision Date | April 05, 2005 |
| Days to Decision | 69 days |
| Submission Type | Traditional |
| Review Panel | Cardiovascular (CV) |
| Summary | Summary PDF |
| Product Code | DQD — Stethoscope, Electronic |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 870.1875 |