Company ยท US
Uromed Corp.
FDA 510(k) clearances and medical device recalls filed under this name, 1997 to 2001. 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 |
|---|---|---|---|
| Apr 20, 2001 | K010213 | MODIFICATION TO CAVERMAP SURGICAL AID Uromed Corp. | ETN |
| Feb 1, 2001 | K010098 | MODIFICATION TO CAVERMAP SURGICAL AID Uromed Corp. | FGM |
| Apr 21, 2000 | K000507 | CAVERMAP SURGICAL AID Uromed Corp. | ETN |
| Feb 11, 2000 | K993436 | CAVERMAP SURGICAL AID Uromed Corp. | FGM |
| May 13, 1999 | K982226 | UROMED BRACHYTHERAPHY IODINE-125 SOURCES Uromed Corp. | KXK |
| May 22, 1998 | K980717 | UROMED SLING KIT Uromed Corp. | KNA |
| Mar 31, 1998 | K974600 | UROMED PATCH Uromed Corp. | MNG |
| Jan 30, 1998 | K974137 | UROMED NEEDLE GRASPER Uromed Corp. | OCW |
| Oct 27, 1997 | K970971 | URO MED NERVE STIMULATOR Uromed Corp. | ETN |
| Aug 1, 1997 | K971992 | UROMED ALTERNATIVE BLADDER CONTROL CONTINENCE DEVICE(ABCPN-0026) Uromed Corp. | FHA |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||