510(k) K833822

P-S MEDICAL CSF ACCESS DEV 15MM/25MM by Pudenz-Schulte Medical Research Corp. — Product Code LKG

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 25, 1984
Date Received
November 2, 1983
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Port & Catheter, Implanted, Subcutaneous, Intraventricular
Device Class
Class II
Regulation Number
882.5550
Review Panel
HO
Submission Type