Minrad, Inc. is one of 15043 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Minrad, Inc. - FDA 510(k) Cleared Devices
Recent clearances: MINRAD INC. NASAL SCAVENGING CIRCUIT, LIGHT SABRE SPINAL ACCESS DEVICE, MR FIBER OPTIC INTUBATING LARYNGOSCOPE HANDLE, SHORT, MODEL 310002
14
Total
14
Cleared
0
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
Cleared
Oct 18, 2007
MINRAD INC. NASAL SCAVENGING CIRCUIT
Anesthesiology
66d
Cleared
Oct 16, 2007
LIGHT SABRE SPINAL ACCESS DEVICE
Gastroenterology & Urology
106d
Cleared
Aug 31, 2006
MR FIBER OPTIC INTUBATING LARYNGOSCOPE HANDLE, SHORT, MODEL 310002
Anesthesiology
29d
Cleared
Aug 31, 2006
MR FIBER OPTIC INTUBATING LARYNGOSCOPE HANDLE, STANDARD, MODEL 310001
Anesthesiology
29d
Cleared
Nov 15, 2004
MR TESTED FIBER OPTIC SHORT LARYNGOSCOPE HANDLE, MODEL 310002
Anesthesiology
130d
Cleared
Aug 26, 2004
SABRESOURCE DRAPE
General Hospital
49d
Cleared
Jul 03, 2002
LIGHT SABER SPINAL NEEDLE
Radiology
90d
Cleared
Dec 07, 2001
LIGHT SABER INTRODUCER NEEDLE
General & Plastic Surgery
88d
Cleared
Sep 09, 1998
LIGHT SABER BONE BIOPSY NEEDLE
Gastroenterology & Urology
35d
Cleared
Aug 07, 1998
LIGHT SABER ASPIRATION NEEDLE
General Hospital
60d
Cleared
Aug 05, 1998
LIGHT SABER CORE TISSUE NEEDLE
Gastroenterology & Urology
76d
Cleared
Jun 25, 1998
MINRAD DRTS LIGHT SABER SYRINGE
General Hospital
87d