Company ยท US
Vxtra Corp.
FDA 510(k) clearances and medical device recalls filed under this name, 1980 to 1983. Name variants (Inc, Corp, punctuation) are merged.
10510(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 |
|---|---|---|---|
| Oct 19, 1983 | K832980 | VXTRA OCUTOME KIT Vxtra Corp. | HQC |
| Oct 19, 1983 | K832938 | OCUTOME PARATUBING SET Vxtra Corp. | |
| Jun 10, 1983 | K831266 | MICROSURGICAL KNIFE Vxtra Corp. | HNN |
| Apr 5, 1983 | K830385 | IRRIGATION/ASPIRATION KIT Vxtra Corp. | HQC |
| Apr 5, 1983 | K830379 | PHAKO KIT Vxtra Corp. | HQC |
| Oct 19, 1981 | K812620 | ADJUSTABLE MICROSURGICAL KNIFE Vxtra Corp. | HNN |
| Sep 16, 1981 | K812526 | MICRO BLADE II Vxtra Corp. | GES |
| Aug 31, 1981 | K812160 | MICROSURGICAL BLADE Vxtra Corp. | GES |
| Apr 21, 1980 | K800557 | DISPOSABLE PRE-GELLED ELECTROSURGICAL Vxtra Corp. | GEI |
| Feb 22, 1980 | K792436 | VXTRA BACK PACK EKG ELECTRODE CAT. NO. Vxtra Corp. | DRX |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||