Company ยท US
Neoprobe Corp.
FDA 510(k) clearances and medical device recalls filed under this name, 1986 to 2005. Name variants (Inc, Corp, punctuation) are merged.
6510(k) clearances (0 in 12 months)
2recalls (0 in 12 months)
2recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Feb 8, 2005 | K050088 | QUANTIX/OR BLOOD FLOW MONITOR; FLEXIBLE PROBE WITH OPTIONAL VESSEL STABILIZER Neoprobe Corp. | DPW |
| Jun 26, 1997 | K971167 | NEOPROBE MODEL 1500 PORTABLE RADIOISOTOPE DETECTOR AND ACCESSORIES Neoprobe Corp. | IZD |
| Sep 13, 1996 | K962319 | NEOPROBE 1000 GEN 1C PORTABLE RADIOISOTOPE DETECTOR & ACCESSORIES Neoprobe Corp. | IZD |
| Feb 9, 1995 | K942580 | NEOPROBE 1000 PORTABLE RADIOISOTOPE DETECTOR AND ACCESSORIES Neoprobe Corp. | IZD |
| Jun 10, 1992 | K915279 | NEOPROBE PORTABLE RADIOSCOPE DETECTOR Neoprobe Corp. | IZD |
| Dec 29, 1986 | K864263 | NEOPROBE PORTABLE RADIOISOTOPE DETECTOR Neoprobe Corp. | IZD |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Apr 13, 2005 | Neoprobe Corp Product is CSN00200 4MHz blood flowmeter probe used with the Quantix/OR system. Terminated |
DPW | K030357 |
| Apr 13, 2005 | Neoprobe Corp Product is CSN00210 8MHz blood flowmeter probe used with the Quantix/OR system. Terminated |
DPW | K030357 |