ClearanceBrief
Company ยท US

Action Products Incorporated

FDA 510(k) clearances and medical device recalls filed under this name, 1980 to 1981. Name variants (Inc, Corp, punctuation) are merged.

2510(k) clearances (0 in 12 months)
4recalls (0 in 12 months)
2recalls that name a 510(k)

Product codes

CodeDeviceRecords
JADSystem, Therapeutic, X-Ray3
FMPProtector, Skin Pressure1
IORWheelchair, Mechanical1
KNOAccessories, Wheelchair1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jul 10, 1981K811528RADIATION BOLUS
Action Products, Inc.
JAD
Aug 27, 1980K801694FLOTATION PAD FOR OPERATING TABLE
Action Products, Inc.
FMP

Latest recalls

DateFirm and productCodeLinked 510(k)
Sep 22, 2009Action Products Incorporated
Action Products, Inc., Bol-X-II, 30x30x1.0cm, item number 32102, packaged 10/carton. Polymer pad used during radiation therapy.
Terminated
JADK811528
Sep 22, 2009Action Products Incorporated
Action Products, Inc., Bol-X-II, 30x30x0.5cm, item number 32052, packaged 10/carton. Polymer pad used during radiation therapy.
Terminated
JADK811528
Jul 20, 2004Action Products Incorporated
Xact(tm) Drop Seat Base, a plastic seat support in Xact (tm) Integrated and Xact Individual w/ Drop seat Base Wheelchair cushions.
Terminated
KNONone listed
May 14, 2003Action Products Incorporated
Twister(tm) Cube Back-Cane Short, a wheelchair back seat support strap, part number WPHS.
Terminated
IORNone listed
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