K153591 is an FDA 510(k) clearance for the ebb Complete Tamponade System. This device is classified as a Intrauterine Tamponade Balloon (Class II - Special Controls, product code OQY).
Submitted by Clinical Innovations, LLC (Murray, US). The FDA issued a Cleared decision on January 14, 2016, 29 days after receiving the submission on December 16, 2015.
This device falls under the Obstetrics & Gynecology FDA review panel. Regulated under 21 CFR 884.4530. Provides Temporary Control Or Reduction Of Postpartum Uterine Bleeding.
| 510(k) Number | K153591 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | December 16, 2015 |
| Decision Date | January 14, 2016 |
| Days to Decision | 29 days |
| Submission Type | Special |
| Review Panel | Obstetrics & Gynecology (OB) |
| Summary | Summary PDF |
| Product Code | OQY - Intrauterine Tamponade Balloon |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 884.4530 |
| Definition | Provides Temporary Control Or Reduction Of Postpartum Uterine Bleeding |