510(k) K945556

ANTERIOR/POSTERIOR EPISTAXIS CATHETER by Ultracell Medical Technologies, Inc. — Product Code EMX

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 18, 1995
Date Received
November 14, 1994
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Balloon, Epistaxis
Device Class
Class I
Regulation Number
874.4100
Review Panel
EN
Submission Type