Re: Product Liability Case To Be Heard Soon

From: art fougner, md (evsono@pipeline.com)
Tue Nov 20 07:07:20 2007


And then there's the ... Commerce Clause ...

Art

At Mon, 19 Nov 2007, DoctorJoe@aol.com wrote: >
>In a message dated 11/19/2007 2:14:42 P.M. Central Standard Time,
>dean@thehuffpeople.net writes:
>
>The MDA generally forbids states from
>imposing requirements on devices that received premarket approval from the
>Food
>and Drug Administration ("FDA").
>
>Well, I think they're toast. The law specifically states that the states
>can't add to the regulation of the device unless there are some "compelling
>local conditions" which would make it necessary. I don't know what "local"
>condition exists that would allow some imposition on an angioplasty device. Maybe
>you think doctors in one state are more spastic than doctors in another and so
>... Naw!
>
>Further, even if there was a good argument for a local difference, the State
>has to formally apply for a waiver and have a hearing, etc. That
>(apparently) hasn't been done.
>
>So avenues are available for reasonable State regulation -- just not done
>and probably not needed in this case. Federal law rules.
>
>At least in my opinion here.
>
>Joe P.

--
art fougner, md
"May The Wings of Liberty Never Lose a Feather." - Jack Burton




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