510(k) K870560

COSMEDTECH CANNULA by Cosmedtech, Inc. — Product Code HHI

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 4, 1987
Date Received
February 10, 1987
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
System, Abortion, Vacuum
Device Class
Class II
Regulation Number
884.5070
Review Panel
OB
Submission Type