Jms North America Corp.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 10
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
| K093637 | JMS BLUNT A. V. FISTULA NEEDLE SET WITH SITE PREPARATION TOOL MODEL 820-5300, 820-6300 AND 820-7300 | February 9, 2010 |
| K082882 | A.V. FISTULA BLUNT NEEDLE SET | January 21, 2009 |
| K070234 | JMS SYSLOC MINI AVF AND APHERESIS NEEDLE SETS | May 22, 2007 |
| K070143 | JMS PLANECTA STOPCOCK | April 10, 2007 |
| K051814 | JMS SYSLOC MINI A.V. FISTULA NEEDLE SET AND APHERESIS NEEDLE SET | August 4, 2005 |
| K032975 | JMS BLOOD TUBING SETS | August 16, 2004 |
| K032977 | JMS BYPASS TUBE | May 25, 2004 |
| K040247 | PLUME SAFETY AVF NEEDLE | March 3, 2004 |
| K030479 | JMS SYSLOC A.V. FISTULA NEEDLE SET, JMS SYSLOC APHERESIS NEEDLE SET | August 18, 2003 |
| K023668 | JMS EXTENSION SET WITH PLANECTA, PLANECTA (STAND ALONE UNIT), PLANECTA LOCK & PLANECTA ADAPTOR | July 1, 2003 |