510(k) K831580

PARAFFIN INFILTRATION MEDIUM by Surgipath Medical Industries, Inc. — Product Code KEO

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 17, 1983
Date Received
May 17, 1983
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Formulations, Paraffin, All
Device Class
Class I
Regulation Number
864.4010
Review Panel
PA
Submission Type