Question No 30:
A company begins to market its new device, a pacemaker (Class III) the same day that its regulatory professional mails the Premaket Approval Application (PMA) to FDA. The pacemaker is considered:A. Legally marketed
B. Misbranded
C. Investigational
D. Adulterated
Answer: D
No comments:
Post a Comment
Note: Only a member of this blog may post a comment.