Company ยท US
Diagnostic Monitoring Software
FDA 510(k) clearances and medical device recalls filed under this name, 1992 to 2014. Name variants (Inc, Corp, punctuation) are merged.
5510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| May 19, 2014 | K133014 | DMS 300-2W HOLTER ECG RECORDER Diagnostic Monitoring Software | MWJ |
| Oct 16, 2006 | K062959 | DMS 300-2, 300-3 AND 300-4 Diagnostic Monitoring Software | MWJ |
| Aug 25, 2006 | K062088 | PREMIER 11 HOLTER Diagnostic Monitoring Software | MLO |
| Aug 16, 2006 | K062007 | DMS 300-7 Diagnostic Monitoring Software | DSH |
| Jan 8, 1992 | K911615 | HOLTER 24-HOUR ECG SYSTEM, MODEL NUMBER: DMS 300 Diagnostic Monitoring Software | DQK |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||