K943456 is an FDA 510(k) clearance for the AS/3 NELLCOR COMPATIBLE SATURATION MOODULE, M-NSAT. This device is classified as a Oximeter (Class II - Special Controls, product code DQA).
Submitted by Datex Division Instrumentarium Corp. (Helsinki, FI). The FDA issued a Cleared decision on October 17, 1994, 91 days after receiving the submission on July 18, 1994.
This device falls under the Anesthesiology FDA review panel. Regulated under 21 CFR 870.2700.
| 510(k) Number | K943456 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | July 18, 1994 |
| Decision Date | October 17, 1994 |
| Days to Decision | 91 days |
| Submission Type | Traditional |
| Review Panel | Anesthesiology (AN) |
| Summary | Summary PDF |
| Product Code | DQA — Oximeter |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 870.2700 |