K092324 is an FDA 510(k) clearance for the SPIROPRO. This device is classified as a Oximeter (Class II - Special Controls, product code DQA).
Submitted by Viasys Healthcare GmbH (Hoechberg, DE). The FDA issued a Cleared decision on September 3, 2009, 30 days after receiving the submission on August 4, 2009.
This device falls under the Anesthesiology FDA review panel. Regulated under 21 CFR 870.2700.
| 510(k) Number | K092324 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | August 04, 2009 |
| Decision Date | September 03, 2009 |
| Days to Decision | 30 days |
| Submission Type | Special |
| Review Panel | Anesthesiology (AN) |
| Summary | Summary PDF |
| Product Code | DQA — Oximeter |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 870.2700 |