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) cleared devices by Minrad, Inc.

14 devices

1-12 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

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

FDA 510(k) cleared devices by Minrad, Inc.

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