ClearanceBrief
Company ยท US

Radius Medical Technologies, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1997 to 2007. Name variants (Inc, Corp, punctuation) are merged.

9510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
DQXWire, Guide, Catheter3
MMXDevice, Percutaneous Retrieval3
DQYCatheter, Percutaneous1
LITCatheter, Angioplasty, Peripheral, Transluminal1
OCYEndoscopic Guidewire, Gastroenterology-Urology1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Oct 4, 2007K070502RADIUS SNARE
Radius Medical Technologies, Inc.
DQY
Sep 25, 2007K071457MODIFICATION TO RADIUS SNARE
Radius Medical Technologies, Inc.
MMX
Oct 17, 2003K032899RADIUS COUGAR WIRE
Radius Medical Technologies, Inc.
DQX
Jul 17, 2003K032129RADIUS 018 COUGAR WIRE
Radius Medical Technologies, Inc.
DQX
Feb 3, 2003K022201RADIUS MICRO SNARE
Radius Medical Technologies, Inc.
MMX
Jun 14, 2002K021441RADIUS SNARE
Radius Medical Technologies, Inc.
MMX
Aug 23, 2001K011759RADIUS NEXT GENERATION GUIDEWIRE
Radius Medical Technologies, Inc.
OCY
May 25, 2001K011287RADIUS COUGAR WIRE
Radius Medical Technologies, Inc.
DQX
May 20, 1997K970466RADIUS PTCA GUIDEWIRE
Radius Medical Technologies, Inc.
LIT

Latest recalls

DateFirm and productCodeLinked 510(k)
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