510(k) K854899

NOVAK CURETTE by Euro-Med Intl. — Product Code FZS

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 24, 1985
Date Received
December 6, 1985
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Curette, Surgical, General Use
Device Class
Class I
Regulation Number
878.4800
Review Panel
SU
Submission Type