Medical Device Manufacturer · US , Washington , DC

Minrad, Inc. - FDA 510(k) Cleared Devices

14 submissions · 14 cleared · Since 1997

Total

Cleared

Denied

Minrad, Inc. has 14 FDA 510(k) cleared medical devices. Based in Washington, US.

Historical record: 14 cleared submissions from 1997 to 2007.

Browse the FDA 510(k) cleared devices submitted by Minrad, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Minrad, Inc.

14 devices

1-14 of 14

Cleared Oct 18, 2007

MINRAD INC. NASAL SCAVENGING CIRCUIT

K072255 · CBN

Anesthesiology · 66d

Cleared Oct 16, 2007

LIGHT SABRE SPINAL ACCESS DEVICE

K071814 · KNW

Gastroenterology & Urology · 106d

Cleared Aug 31, 2006

MR FIBER OPTIC INTUBATING LARYNGOSCOPE HANDLE, SHORT, MODEL 310002

K062230 · CCW

Anesthesiology · 29d

Cleared Aug 31, 2006

MR FIBER OPTIC INTUBATING LARYNGOSCOPE HANDLE, STANDARD, MODEL 310001

K062231 · CCW

Anesthesiology · 29d

Cleared Nov 15, 2004

MR TESTED FIBER OPTIC SHORT LARYNGOSCOPE HANDLE, MODEL 310002

K041852 · CCW

Anesthesiology · 130d

Cleared Aug 26, 2004

SABRESOURCE DRAPE

K041846 · KKX

General Hospital · 49d

Cleared Jul 03, 2002

LIGHT SABER SPINAL NEEDLE

K021084 · FMF

Radiology · 90d

Cleared Dec 07, 2001

LIGHT SABER INTRODUCER NEEDLE

K013040 · MDM

General & Plastic Surgery · 88d

Cleared Sep 09, 1998

LIGHT SABER BONE BIOPSY NEEDLE

K982735 · KNW

Gastroenterology & Urology · 35d

Cleared Aug 07, 1998

LIGHT SABER ASPIRATION NEEDLE

K982018 · FMF

General Hospital · 60d

Cleared Aug 05, 1998

LIGHT SABER CORE TISSUE NEEDLE

K981796 · KNW

Gastroenterology & Urology · 76d

Cleared Jun 25, 1998

MINRAD DRTS LIGHT SABER SYRINGE

K981140 · FMF

General Hospital · 87d

Cleared Oct 16, 1997

DRTS REMOTE CONTROL DRAPE

K973067 · JAA

Radiology · 59d

Cleared Oct 08, 1997

DRTS IMAGE INTENSIFIER DRAPE

K973073 · JAA

Radiology · 51d

Minrad, Inc. - FDA 510(k) Cleared Devices

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