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Minrad, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
14
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K072255MINRAD INC. NASAL SCAVENGING CIRCUITOctober 18, 2007
K071814LIGHT SABRE SPINAL ACCESS DEVICEOctober 16, 2007
K062231MR FIBER OPTIC INTUBATING LARYNGOSCOPE HANDLE, STANDARD, MODEL 310001August 31, 2006
K062230MR FIBER OPTIC INTUBATING LARYNGOSCOPE HANDLE, SHORT, MODEL 310002August 31, 2006
K041852MR TESTED FIBER OPTIC SHORT LARYNGOSCOPE HANDLE, MODEL 310002November 15, 2004
K041846SABRESOURCE DRAPEAugust 26, 2004
K021084LIGHT SABER SPINAL NEEDLEJuly 3, 2002
K013040LIGHT SABER INTRODUCER NEEDLEDecember 7, 2001
K982735LIGHT SABER BONE BIOPSY NEEDLESeptember 9, 1998
K982018LIGHT SABER ASPIRATION NEEDLEAugust 7, 1998
K981796LIGHT SABER CORE TISSUE NEEDLEAugust 5, 1998
K981140MINRAD DRTS LIGHT SABER SYRINGEJune 25, 1998
K973067DRTS REMOTE CONTROL DRAPEOctober 16, 1997
K973073DRTS IMAGE INTENSIFIER DRAPEOctober 8, 1997