K122539 is an FDA 510(k) clearance for the MEASUREMENT OF PH IN PLEURAL FLUID ON BLOOD GAS SYSTEM. This device is classified as a Electrode Measurement, Blood-gases (pco2, Po2) And Blood Ph (Class II - Special Controls, product code CHL).
Submitted by Siemens Healthcare Diagnostics (Norowood, US). The FDA issued a Cleared decision on April 19, 2013, 241 days after receiving the submission on August 21, 2012.
This device falls under the Chemistry FDA review panel. Regulated under 21 CFR 862.1120.
| 510(k) Number | K122539 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | August 21, 2012 |
| Decision Date | April 19, 2013 |
| Days to Decision | 241 days |
| Submission Type | Traditional |
| Review Panel | Chemistry (CH) |
| Summary | Summary PDF |
| Product Code | CHL — Electrode Measurement, Blood-gases (pco2, Po2) And Blood Ph |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 862.1120 |