K812943 is an FDA 510(k) clearance for the SLICK ENDOTRACHEAL TUBE. This device is classified as a Tube, Tracheal (w/wo Connector) (Class II - Special Controls, product code BTR).
Submitted by Polamedco, Inc. (Mchenry, US). The FDA issued a Cleared decision on November 6, 1981, 17 days after receiving the submission on October 20, 1981.
This device falls under the Anesthesiology FDA review panel. Regulated under 21 CFR 868.5730.
| 510(k) Number | K812943 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | October 20, 1981 |
| Decision Date | November 06, 1981 |
| Days to Decision | 17 days |
| Submission Type | Traditional |
| Review Panel | Anesthesiology (AN) |
| Summary | — |
| Product Code | BTR — Tube, Tracheal (w/wo Connector) |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 868.5730 |