Company ยท US
Minrad, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1997 to 2007. Name variants (Inc, Corp, punctuation) are merged.
14510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Oct 18, 2007 | K072255 | MINRAD INC. NASAL SCAVENGING CIRCUIT Minrad, Inc. | CBN |
| Oct 16, 2007 | K071814 | LIGHT SABRE SPINAL ACCESS DEVICE Minrad, Inc. | KNW |
| Aug 31, 2006 | K062231 | MR FIBER OPTIC INTUBATING LARYNGOSCOPE HANDLE, STANDARD, MODEL 310001 Minrad, Inc. | CCW |
| Aug 31, 2006 | K062230 | MR FIBER OPTIC INTUBATING LARYNGOSCOPE HANDLE, SHORT, MODEL 310002 Minrad, Inc. | CCW |
| Nov 15, 2004 | K041852 | MR TESTED FIBER OPTIC SHORT LARYNGOSCOPE HANDLE, MODEL 310002 Minrad, Inc. | CCW |
| Aug 26, 2004 | K041846 | SABRESOURCE DRAPE Minrad, Inc. | KKX |
| Jul 3, 2002 | K021084 | LIGHT SABER SPINAL NEEDLE Minrad, Inc. | FMF |
| Dec 7, 2001 | K013040 | LIGHT SABER INTRODUCER NEEDLE Minrad, Inc. | MDM |
| Sep 9, 1998 | K982735 | LIGHT SABER BONE BIOPSY NEEDLE Minrad, Inc. | KNW |
| Aug 7, 1998 | K982018 | LIGHT SABER ASPIRATION NEEDLE Minrad, Inc. | FMF |
| Aug 5, 1998 | K981796 | LIGHT SABER CORE TISSUE NEEDLE Minrad, Inc. | KNW |
| Jun 25, 1998 | K981140 | MINRAD DRTS LIGHT SABER SYRINGE Minrad, Inc. | FMF |
| Oct 16, 1997 | K973067 | DRTS REMOTE CONTROL DRAPE Minrad, Inc. | JAA |
| Oct 8, 1997 | K973073 | DRTS IMAGE INTENSIFIER DRAPE Minrad, Inc. | JAA |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||