Company ยท US
Promedical , Ltd.
FDA 510(k) clearances and medical device recalls filed under this name, 1994 to 1995. 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 |
|---|---|---|---|
| Oct 7, 1995 | K954596 | PRO-B CORE-RECT COAXIAL BIOPSY SYSTEM Promedical , Ltd. | FCG |
| Jul 17, 1995 | K952350 | JAMSHIDI STYLE BIOPSY NEEDLE (ACRI) (BIOMID), ILLINOIS STYLE BIOPSY NEEDLE (ISAN) Promedical , Ltd. | LWE |
| Apr 21, 1995 | K951598 | PRO-B BIOPSY NEEDLE Promedical , Ltd. | FCG |
| Dec 21, 1994 | K944944 | CHIBA, FRANSEEN, WESTCOTT, SPINAL STYLE ASPIRATION BIOPSY NEEDLE Promedical , Ltd. | FCG |
| Nov 4, 1994 | K944942 | BREAST LESION LOCALIZATION NEEDLE Promedical , Ltd. | GDF |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||