Douglas Medical Products Corp.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 20
- Inspections
- 2
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K162951 | TUBETECH IV Administration Set | July 28, 2017 |
| K961155 | SOLO PICC/MIDLINE CATHETER KIT MODELS 71924, 71908 | June 18, 1996 |
| K954428 | SOLOPICC 24 (60CM) 20GA CATHETER | March 28, 1996 |
| K941628 | 40 MICRON BLOOD TRANSFUSION FILTER | February 16, 1995 |
| K942101 | 4-LEAD IRRIGATION SET | September 30, 1994 |
| K941453 | CHECK VALVE SOLUTION SET | August 16, 1994 |
| K930854 | SOLUTION SET WITH .2 MICRON FILTER | January 14, 1994 |
| K932637 | SUBCUTANEOUS INFUSION SET | January 7, 1994 |
| K931659 | 3 LEAD CONNECTOR | January 7, 1994 |
| K931658 | IN-LINE BURETTE SET | December 21, 1993 |
| K932638 | HUBER NEEDLE INFUSION SET | December 14, 1993 |
| K932640 | EVA EMPTY MIXING CONTAINER | November 10, 1993 |
| K932641 | EMPTY MIXING CONTAINER | November 10, 1993 |
| K925430 | LO-PROFILE EXTENSIONSET W/ .22 MICRON FILTER | August 3, 1993 |
| K930855 | REPLACEMENT CAP | July 30, 1993 |
| K926184 | DOUGLAS MEDICAL PRODUCTS, INC. VENTED SPIKE ADAPT | July 27, 1993 |
| K921391 | SOLUTION ADMINISTRATION SET | September 2, 1992 |
| K922318 | DOUGLAS MEDICAL PRODUCTS, INC. IRRIGATION SET | August 10, 1992 |
| K920788 | BLOOD ADMINISTRATION SET | June 4, 1992 |
| K915560 | LO-PROFILE EXTENSION SET | May 14, 1992 |