Atrion Medical Products, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 9
- Inspections
- 5
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K060643 | QL LOCKING SYRINGE | July 12, 2006 |
| K043249 | ATRION NEEDLEVISE LARGE-BORE SHARPS SECURING DEVICE | May 25, 2005 |
| K041158 | ATRION EPIDURAL ANESTHESIA KIT WITH ATRION NEEDLEVISE SHARPS SECURING SYSTEM | June 16, 2004 |
| K032840 | ATRION MEDICAL QL INFLATION DEVICE | March 3, 2004 |
| K020333 | ATRION MEDICAL QL FLUID DISPENSING SYRINGE | April 25, 2002 |
| K973633 | ATRION MEDICAL PRODUCTS LACRIMAL INTUBATION SET | January 16, 1998 |
| K973872 | ATRION MEDICAL COATED LACRIMAL INTUBATION SET | January 8, 1998 |
| K972964 | ATRION MEDICAL BALLOON CATHETER INFLATION DEVICE | October 10, 1997 |
| K971100 | ATRION MEDICAL AUTOGENOUS TISSUE COLLECTOR | May 23, 1997 |