K182749 is an FDA 510(k) clearance for the Lansinoh Signature Pro Double Electric Breast Pump, Lansinoh Smartpump Double Electric Breast Pump. This device is classified as a Pump, Breast, Powered (Class II - Special Controls, product code HGX).
Submitted by Lansinoh Laboratories Saglik Gerecleri Tasarim San. Tic., Ltd. (Cigli, TR). The FDA issued a Cleared decision on June 12, 2019, 257 days after receiving the submission on September 28, 2018.
This device falls under the Obstetrics & Gynecology FDA review panel. Regulated under 21 CFR 884.5160.
| 510(k) Number | K182749 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | September 28, 2018 |
| Decision Date | June 12, 2019 |
| Days to Decision | 257 days |
| Submission Type | Traditional |
| Review Panel | Obstetrics & Gynecology (OB) |
| Summary | Summary PDF |
| Product Code | HGX - Pump, Breast, Powered |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 884.5160 |