ClearanceBrief
Company ยท US

Dyna Corp.

FDA 510(k) clearances and medical device recalls filed under this name, 1990 to 1997. Name variants (Inc, Corp, punctuation) are merged.

5510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
FPOStretcher, Wheeled3
FPPStretcher, Hand-Carried2

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jul 28, 1997K972528DYNA GLIDE 2600 ROLL-IN AMBULANCE COT (95759)
Dyna Corp.
FPO
Aug 1, 1996K962181HARE MODEL 2000 EZ LOADER MODEL 95555
Dyna Corp.
FPO
Jun 26, 1990K902503HARE FOLDING BACK EMERGENCY STRETCHER
Dyna Corp.
FPO
Apr 23, 1990K900671HARE EMERGENCY STRETCHER WITH WHEELS
Dyna Corp.
FPP
Apr 23, 1990K900670HARE EMERGENCY STRETCHER
Dyna Corp.
FPP

Latest recalls

DateFirm and productCodeLinked 510(k)
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