K890058 is an FDA 510(k) clearance for the VASCULAR TECHNOLOGY UNIOX OXYGEN ALARM. This device is classified as a Analyzer, Gas, Oxygen, Gaseous-phase (Class II - Special Controls, product code CCL).
Submitted by Vascular Technology Incorporated (Chelmsford, US). The FDA issued a Cleared decision on November 21, 1989, 319 days after receiving the submission on January 6, 1989.
This device falls under the Anesthesiology FDA review panel. Regulated under 21 CFR 868.1720.
| 510(k) Number | K890058 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | January 06, 1989 |
| Decision Date | November 21, 1989 |
| Days to Decision | 319 days |
| Submission Type | Traditional |
| Review Panel | Anesthesiology (AN) |
| Summary | — |
| Product Code | CCL — Analyzer, Gas, Oxygen, Gaseous-phase |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 868.1720 |