Company ยท US
Myotronics-Noromed, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1999 to 2011. Name variants (Inc, Corp, punctuation) are merged.
7510(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 |
|---|---|---|---|
| Sep 29, 2011 | K111687 | EMG SYSTEM Myotronics-Noromed, Inc. | HCC |
| Jul 20, 2004 | K040400 | MYO-TRODE SG DISPOSABLE ELECTRODE Myotronics-Noromed, Inc. | NUW |
| Jul 24, 2003 | K031998 | MODEL J-5 MVO-MONITOR Myotronics-Noromed, Inc. | NUW |
| Nov 13, 2001 | K013399 | MODEL MES-9000/EMG SYSTEM Myotronics-Noromed, Inc. | HCC |
| Nov 6, 2000 | K003287 | MODEL K7 EVALUATION DEVICE Myotronics-Noromed, Inc. | KZM |
| Sep 10, 1999 | K992694 | MODIFICATION TO K6-I DIAGNOSTIC SYSTEM, MODEL K6-I Myotronics-Noromed, Inc. | KZM |
| Aug 13, 1999 | K992439 | NORODYN 8000 SEMG SYSTEM, ND-8000 Myotronics-Noromed, Inc. | HCC |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||