Bioelectronics Corp (BIEL)

[nomonet]

Most often it depends on the type of devices and type of submission. Also it depends on the clinical data and the regulatory group putting the data together that has a bearing.
Typically on simple devices is ranges from my experience 3-6 months depending on the FDA questions. You always get questions back.

To add prospective.....here is a Reuter's link that might help.

http://www.reuters.com/article/healthNews/idUSWBT00924520080623