K020494 is an FDA 510(k) clearance for the MODIFICATION TO M2376A DEVICELINK SYSTEM. This device is classified as a Monitor, Physiological, Patient (without Arrhythmia Detection Or Alarms) (Class II - Special Controls, product code MWI).
Submitted by Philips Medical Systems, Inc. (Andover, US). The FDA issued a Cleared decision on February 21, 2002, 8 days after receiving the submission on February 13, 2002.
This device falls under the Cardiovascular FDA review panel. Regulated under 21 CFR 870.2300.
| 510(k) Number | K020494 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | February 13, 2002 |
| Decision Date | February 21, 2002 |
| Days to Decision | 8 days |
| Submission Type | Special |
| Review Panel | Cardiovascular (CV) |
| Summary | Summary PDF |
| Product Code | MWI — Monitor, Physiological, Patient (without Arrhythmia Detection Or Alarms) |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 870.2300 |