Company ยท DK
Unoplast A/S
FDA 510(k) clearances and medical device recalls filed under this name, 1980 to 1990. Name variants (Inc, Corp, punctuation) are merged.
7510(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 |
|---|---|---|---|
| Dec 21, 1990 | K896734 | FEEDING TUBE Unoplast A/S, DK | FPD |
| Nov 5, 1990 | K896729 | NELATON-, FEMALE - OR TIEMANN CATHETER Unoplast A/S, DK | KOD |
| Nov 2, 1990 | K896732 | UNOMETER 500 Unoplast A/S, DK | EXR |
| Mar 30, 1990 | K896731 | OXYGEN CATHETERS Unoplast A/S, DK | BZB |
| Mar 30, 1990 | K896730 | SUCTION CATHETER STRAIGHT/COUDE Unoplast A/S, DK | BSY |
| Feb 1, 1990 | K896733 | VACCON Unoplast A/S, DK | KGX |
| Sep 26, 1980 | K802248 | DISARP ORIGINAL Unoplast A/S | GAO |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||