Minrad, Inc.
Minrad, Inc. holds FDA 510(k) medical device clearances, first cleared 1997, most recent 2007.
Top product codes for Minrad, Inc.
Recent clearances by Minrad, Inc.
- K072255 — MINRAD INC. NASAL SCAVENGING CIRCUIT
- K071814 — LIGHT SABRE SPINAL ACCESS DEVICE
- K062230 — MR FIBER OPTIC INTUBATING LARYNGOSCOPE HANDLE, SHORT, MODEL 310002
- K062231 — MR FIBER OPTIC INTUBATING LARYNGOSCOPE HANDLE, STANDARD, MODEL 310001
- K041852 — MR TESTED FIBER OPTIC SHORT LARYNGOSCOPE HANDLE, MODEL 310002
- K041846 — SABRESOURCE DRAPE
- K021084 — LIGHT SABER SPINAL NEEDLE
- K013040 — LIGHT SABER INTRODUCER NEEDLE
- K982735 — LIGHT SABER BONE BIOPSY NEEDLE
- K982018 — LIGHT SABER ASPIRATION NEEDLE
- K981796 — LIGHT SABER CORE TISSUE NEEDLE
- K981140 — MINRAD DRTS LIGHT SABER SYRINGE
- K973067 — DRTS REMOTE CONTROL DRAPE
- K973073 — DRTS IMAGE INTENSIFIER DRAPE
Data sourced from openFDA. This site is unofficial and independent of the FDA.