Minrad, Inc.
Washington, DC, US
Minrad, Inc. appears in FDA device records in Washington, DC. FDA records list 14 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 14
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 14 510(k) clearances for Minrad, Inc. between 1997 and 2007. The busiest year on record is 1998, with 4. The most recent is 2007, with 2.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1997 | 2 |
| 1998 | 4 |
| 2001 | 1 |
| 2002 | 1 |
| 2004 | 2 |
| 2006 | 2 |
| 2007 | 2 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K072255 | MINRAD INC. NASAL SCAVENGING CIRCUIT | CBN | Substantially Equivalent | |
| K071814 | LIGHT SABRE SPINAL ACCESS DEVICE | KNW | Substantially Equivalent | |
| K062231 | MR FIBER OPTIC INTUBATING LARYNGOSCOPE HANDLE, STANDARD, MODEL 310001 | CCW | Substantially Equivalent | |
| K062230 | MR FIBER OPTIC INTUBATING LARYNGOSCOPE HANDLE, SHORT, MODEL 310002 | CCW | Substantially Equivalent | |
| K041852 | MR TESTED FIBER OPTIC SHORT LARYNGOSCOPE HANDLE, MODEL 310002 | CCW | Substantially Equivalent | |
| K041846 | SABRESOURCE DRAPE | KKX | Substantially Equivalent | |
| K021084 | LIGHT SABER SPINAL NEEDLE | FMF | Substantially Equivalent | |
| K013040 | LIGHT SABER INTRODUCER NEEDLE | MDM | Substantially Equivalent | |
| K982735 | LIGHT SABER BONE BIOPSY NEEDLE | KNW | Substantially Equivalent | |
| K982018 | LIGHT SABER ASPIRATION NEEDLE | FMF | Substantially Equivalent | |
| K981796 | LIGHT SABER CORE TISSUE NEEDLE | KNW | Substantially Equivalent | |
| K981140 | MINRAD DRTS LIGHT SABER SYRINGE | FMF | Substantially Equivalent | |
| K973067 | DRTS REMOTE CONTROL DRAPE | JAA | Substantially Equivalent | |
| K973073 | DRTS IMAGE INTENSIFIER DRAPE | JAA | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain