K030939 is an FDA 510(k) clearance for the PHILIPS COMPURECORD PERI-OPERATIVE INFORMATION SYSTEM SOFTWARE. This device is classified as a Gas-machine, Anesthesia (Class II - Special Controls, product code BSZ).
Submitted by Philips Medical Systems (Pittsburgh, US). The FDA issued a Cleared decision on July 15, 2003, 112 days after receiving the submission on March 25, 2003.
This device falls under the Anesthesiology FDA review panel. Regulated under 21 CFR 868.5160.
| 510(k) Number | K030939 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | March 25, 2003 |
| Decision Date | July 15, 2003 |
| Days to Decision | 112 days |
| Submission Type | Special |
| Review Panel | Anesthesiology (AN) |
| Summary | Summary PDF |
| Product Code | BSZ — Gas-machine, Anesthesia |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 868.5160 |