Medi-Craft , Ltd.
Medi-Craft , Ltd. appears in FDA public data with 0 recalls, 9 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on October 22, 1986.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 9
- Inspections
- 0
- Compliance Actions
- 0
Known Names
medicraft, medi-craft
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K861949 | SUCTION CATHETER KIT | October 22, 1986 |
| K800510 | RECTAL & HARRIS FLUSH TUBES | April 8, 1980 |
| K800507 | FEEDING TUBES | April 8, 1980 |
| K800505 | URETHRAL CATHETER | April 8, 1980 |
| K800508 | STOMACH TUBES | April 8, 1980 |
| K800509 | CONNECTING TUBES | March 25, 1980 |
| K800506 | OXYGEN CATHETER | March 25, 1980 |
| K800503 | SUCTION CATHETER | March 18, 1980 |
| K800504 | OXYGEN CONNECTING TUBES | March 18, 1980 |