Anonymous
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Anonymous
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Nope...wrong again. CE Mark approval comes first, then submission to FDA...in this case anyway.
Nope...wrong again. CE Mark approval comes first, then submission to FDA...in this case anyway.
So you win the discussion with information that puts the X-Porte available in Dec./Janarary
Ok, everything is fine, no worries
Ok. Now you know who I am now, like I said. Seek me out in August.
If I don't have a clue, maybe you can enlighten me!
This is all the time I have for this. See you in LA!
Ok mate, what do you have to say now?
It's a bull shit machine. Here comes another big helping
Relax, carry on, everything is fine. Best ultrasound system ever produced.
You are about to enjoy a 4-5 year run before anything from the competition comes close.
That is some funny shit there. This company has not done anything right in 4 years, what makes you think this is going to be any different??? The fact the deadlines are all BS should tell you its another Titanic fart
^^^^^ wrong, many things done well. That's why Sonosite is the leader and will continue to be so.
Part of the success has been eliminating dead wood. You have either been canned in recent RIF or will be , due to lack of performance.
Nope, neither apply. Just seen enough to know this place is a shadow of what it once was.
I wish we were still the leader of the pack, but no one here remembers what "good" even is anymore. how bout management just meets ONE commitment for a change
I have to agree. We have been fed so much misinformation about the x-poop. It's pretty hard to believe anything management says at this point. Remember them saying AUGUST for SURE!!
Congrats to all the reps in Europe....what about the rest of us!
Don't worry you will have it by January
GREAT NEWS!
That's January 2015
Not credible. Stop wasting time.
Congrats to all the reps in Europe....what about the rest of us!
After our time in LA, and understanding when this will have FDA clearance, I'm whelmed, but not overly.
http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfPMN/pmn.cfm
Where is the 510(k) pre-market submission?