Burron Medical Products, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 41
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K870403 | CAVAFIX(R) CENTRAL VENOUS CATHETER KIT W/SUTURE | May 1, 1987 |
| K862412 | INTESTOPLANT | November 13, 1986 |
| K861479 | CAVAFIX, CENTRAL VENOUS CATHETER KIT | July 1, 1986 |
| K860126 | STIMUPLEX, NERVE STIMULATOR | February 28, 1986 |
| K851293 | IMPLANTOFIX | January 9, 1986 |
| K841428 | JEJUNOSTOMY SET FOR TUBE FEEDING | July 9, 1984 |
| K834299 | LONG TERM CENTRAL VENOUS ACCESS CATH | May 1, 1984 |
| K834383 | DUAL-LUMEN LONG TERM CENTRAL VENOUS CAT | May 1, 1984 |
| K834473 | MULTI-LUMEN CENTRAL VENOUS CATH. KIT | April 30, 1984 |
| K840179 | CONTINUOUS EPIDURAL ANESTHES. TRAY | February 24, 1984 |
| K840287 | BRACHIAL PLEXUS ANESTHESIA TRAY | February 23, 1984 |
| K830571 | BOTTLE ADAPTER | March 24, 1983 |
| K830572 | CLEAN-FLUSH | March 17, 1983 |
| K830193 | CAT 3040 | March 9, 1983 |
| K820453 | THE INT-STOPPER | March 8, 1982 |
| K820454 | THE RED CAP | March 8, 1982 |
| K820004 | PLEUROFIX THORACENTESIS KIT | February 4, 1982 |
| K820047 | SPINOCAN SPINAL NEEDLE | January 25, 1982 |
| K813396 | VERSCHLUBSTOPFEN COMB-CLOSING STOPPER | January 12, 1982 |
| K813498 | MEDIFIX | January 7, 1982 |