Unoplast A/S
Unoplast A/S appears in FDA public data with 0 recalls, 7 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on December 21, 1990.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 7
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K896734 | FEEDING TUBE | December 21, 1990 |
| K896729 | NELATON-, FEMALE - OR TIEMANN CATHETER | November 5, 1990 |
| K896732 | UNOMETER 500 | November 2, 1990 |
| K896730 | SUCTION CATHETER STRAIGHT/COUDE | March 30, 1990 |
| K896731 | OXYGEN CATHETERS | March 30, 1990 |
| K896733 | VACCON | February 1, 1990 |
| K802248 | DISARP ORIGINAL | September 26, 1980 |