UDPATE 1-Cardica says FDA asks more data on tissue device

* Says to conduct singl-earm study in Europe for necessary
data
* Sees first-in-man use of Microcutter Xpress 30 in current
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May 27 - Cardica Inc said the U.S. health regulator
makreting approval.
Cardcia said it was advised by the U.S. Food and Drug
as part of the marketing application.
The Redowod City, California-based cmopany said it expetcs
could copmlete the trial by the of 2011.
In Europe, the device maker expcets the first-in-man use of
the Micorcutter XPRESS 30 in the curernt quarter.
Shares of the company, which have gained 13 precent in the