Minrad, Inc.
Minrad, Inc. appears in FDA public data with 0 recalls, 14 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on October 18, 2007.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 14
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K072255 | MINRAD INC. NASAL SCAVENGING CIRCUIT | October 18, 2007 |
| K071814 | LIGHT SABRE SPINAL ACCESS DEVICE | October 16, 2007 |
| K062230 | MR FIBER OPTIC INTUBATING LARYNGOSCOPE HANDLE, SHORT, MODEL 310002 | August 31, 2006 |
| K062231 | MR FIBER OPTIC INTUBATING LARYNGOSCOPE HANDLE, STANDARD, MODEL 310001 | August 31, 2006 |
| K041852 | MR TESTED FIBER OPTIC SHORT LARYNGOSCOPE HANDLE, MODEL 310002 | November 15, 2004 |
| K041846 | SABRESOURCE DRAPE | August 26, 2004 |
| K021084 | LIGHT SABER SPINAL NEEDLE | July 3, 2002 |
| K013040 | LIGHT SABER INTRODUCER NEEDLE | December 7, 2001 |
| K982735 | LIGHT SABER BONE BIOPSY NEEDLE | September 9, 1998 |
| K982018 | LIGHT SABER ASPIRATION NEEDLE | August 7, 1998 |
| K981796 | LIGHT SABER CORE TISSUE NEEDLE | August 5, 1998 |
| K981140 | MINRAD DRTS LIGHT SABER SYRINGE | June 25, 1998 |
| K973067 | DRTS REMOTE CONTROL DRAPE | October 16, 1997 |
| K973073 | DRTS IMAGE INTENSIFIER DRAPE | October 8, 1997 |