ClearanceBrief
Company ยท CA

Pdg Product Design Group, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1996 to 2017. Name variants (Inc, Corp, punctuation) are merged.

8510(k) clearances (0 in 12 months)
1recalls (0 in 12 months)
1recalls that name a 510(k)

Product codes

CodeDeviceRecords
IORWheelchair, Mechanical9

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jun 27, 2017K163432Stellar LEAP
Pdg Product Design Group, Inc., CA
IOR
Oct 16, 2014K140023ELEVATION
Pdg Product Design Group, Inc.
IOR
Jan 17, 2007K063736FUZE MECHANICAL WHEELCHAIR, MODELS T20 AND T50
Pdg Product Design Group, Inc.
IOR
Jun 14, 2006K061475ASTROTILT MANUAL WHEELCHAIR
Pdg Product Design Group, Inc., CA
IOR
Mar 22, 1999K990557THE STELLAR TILT, MANUALLY OPERATED WHEELCHAIR
Pdg Product Design Group, Inc., CA
IOR
May 9, 1997K971389ECLIPSE 400 MANUALLY OPERATED WHEELCAIR
Pdg Product Design Group, Inc., CA
IOR
Feb 14, 1997K970311BENTLEY MANUALLY OPERATED WHEELCHAIR
Pdg Product Design Group, Inc., CA
IOR
May 29, 1996K961743ECLIPSE 600 MANUALLY OPERATED WHEELCHAIR
Pdg Product Design Group, Inc., CA
IOR

Latest recalls

DateFirm and productCodeLinked 510(k)
Sep 24, 2014Pdg Product Design Group Inc
Fuze Manual Tilt Wheelchair. Fuze T50, Fuze T20 and Fuze T50 Jr
Terminated
IORK063736
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