K131626 is an FDA 510(k) clearance for the EXCELERON BACTERIAL FILTERS. This device is classified as a Filter, Bacterial, Breathing-circuit (Class II — Special Controls, product code CAH).
Submitted by Exceleron Medical (St. Paul, US). The FDA issued a Cleared decision on February 26, 2014, 267 days after receiving the submission on June 4, 2013.
This device falls under the General Hospital FDA review panel. Regulated under 21 CFR 868.5260.
| 510(k) Number | K131626 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | June 04, 2013 |
| Decision Date | February 26, 2014 |
| Days to Decision | 267 days |
| Submission Type | Traditional |
| Review Panel | General Hospital (HO) |
| Summary | Summary PDF |
| Product Code | CAH — Filter, Bacterial, Breathing-circuit |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 868.5260 |