K153681 is an FDA 510(k) clearance for the PleuraFlow System. This device is classified as a Wound Drain Catheter System (Class II - Special Controls, product code OTK).
Submitted by Clearflow, Inc. (Anaheim, US). The FDA issued a Cleared decision on January 20, 2016, 29 days after receiving the submission on December 22, 2015.
This device falls under the General & Plastic Surgery FDA review panel. Regulated under 21 CFR 878.4780. For Use As An Adjunctive Device During Open Surgical Procedures In Order To Prevent Fluid Accumulation Within The Operative Site After Closure Of The Surgical Wound. The Device Is Indicated For Use In Thoracic Surgical Procedures..
| 510(k) Number | K153681 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | December 22, 2015 |
| Decision Date | January 20, 2016 |
| Days to Decision | 29 days |
| Submission Type | Special |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | Summary PDF |
| Product Code | OTK - Wound Drain Catheter System |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 878.4780 |
| Definition | For Use As An Adjunctive Device During Open Surgical Procedures In Order To Prevent Fluid Accumulation Within The Operative Site After Closure Of The Surgical Wound. The Device Is Indicated For Use In Thoracic Surgical Procedures. |