K930004 is an FDA 510(k) clearance for the ESCORT 100/300 SERIES B PATIENT MONITORS. This device is classified as a Monitor, Cardiac (incl. Cardiotachometer & Rate Alarm) (Class II - Special Controls, product code DRT).
Submitted by Medical Data Electronics (Arleta, US). The FDA issued a Cleared decision on June 23, 1993, 170 days after receiving the submission on January 4, 1993.
This device falls under the Cardiovascular FDA review panel. Regulated under 21 CFR 870.2300.
| 510(k) Number | K930004 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | January 04, 1993 |
| Decision Date | June 23, 1993 |
| Days to Decision | 170 days |
| Submission Type | Traditional |
| Review Panel | Cardiovascular (CV) |
| Summary | Statement |
| Product Code | DRT — Monitor, Cardiac (incl. Cardiotachometer & Rate Alarm) |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 870.2300 |