K910509 is an FDA 510(k) clearance for the PATIENT GAS SAMPLING LINE FOR OHMEDA 6000. This device is classified as a Analyzer, Gas, Carbon-dioxide, Gaseous-phase (Class II - Special Controls, product code CCK).
Submitted by Intertech Resources, Inc. (Fort Myers, US). The FDA issued a Cleared decision on April 17, 1991, 71 days after receiving the submission on February 5, 1991.
This device falls under the Anesthesiology FDA review panel. Regulated under 21 CFR 868.1400.
| 510(k) Number | K910509 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | February 05, 1991 |
| Decision Date | April 17, 1991 |
| Days to Decision | 71 days |
| Submission Type | Traditional |
| Review Panel | Anesthesiology (AN) |
| Summary | — |
| Product Code | CCK — Analyzer, Gas, Carbon-dioxide, Gaseous-phase |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 868.1400 |