Company ยท US
Prothia USA, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1982 to 1983. 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 |
|---|---|---|---|
| Jun 8, 1983 | K831071 | UNIVERSAL INSTRU. SET FOR NEUROVASCULAR Prothia USA, Inc. | GZX |
| May 3, 1983 | K830993 | AMPLIGREFFE Prothia USA, Inc. | GFD |
| Mar 24, 1983 | K823581 | ELPHA 500 Prothia USA, Inc. | GCJ |
| Mar 7, 1983 | K830058 | MYOGRAPH 2000 Prothia USA, Inc. | BXN |
| Dec 30, 1982 | K823583 | MYOTEST NERVE STIMULATOR Prothia USA, Inc. | BXN |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||