K761195 is an FDA 510(k) clearance for the ESOPHAGEAL OBTURATION AIRWAY. This device is classified as a Airway, Esophageal (obturator) (Class II - Special Controls, product code CAO).
Submitted by Mckesson Corp. (Mchenry, US). The FDA issued a Cleared decision on December 9, 1976, 3 days after receiving the submission on December 6, 1976.
This device falls under the Anesthesiology FDA review panel. Regulated under 21 CFR 868.5650.
| 510(k) Number | K761195 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | December 06, 1976 |
| Decision Date | December 09, 1976 |
| Days to Decision | 3 days |
| Submission Type | Traditional |
| Review Panel | Anesthesiology (AN) |
| Summary | — |
| Product Code | CAO — Airway, Esophageal (obturator) |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 868.5650 |