K843993 is an FDA 510(k) clearance for the ANAESLOCK THREE VAPORIZER INTERLOCK HVA003. This device is classified as a Vaporizer, Anesthesia, Non-heated (Class II - Special Controls, product code CAD).
Submitted by Southmedic, Inc. (Ancaster, Ontario, CA). The FDA issued a Cleared decision on November 15, 1984, 35 days after receiving the submission on October 11, 1984.
This device falls under the Anesthesiology FDA review panel. Regulated under 21 CFR 868.5880.
| 510(k) Number | K843993 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | October 11, 1984 |
| Decision Date | November 15, 1984 |
| Days to Decision | 35 days |
| Submission Type | Traditional |
| Review Panel | Anesthesiology (AN) |
| Summary | — |
| Product Code | CAD — Vaporizer, Anesthesia, Non-heated |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 868.5880 |