510(k) K020728

Device
MIETHKE SHUNT SYSTEM
Applicant
Aesculap, Inc.
510(k) number
K020728
Product code
HCA
Decision
Substantially Equivalent (SESE)
Decision date
2002-04-05
Date received
2002-03-06
Regulation
882.4100
Classification name
Catheter, Ventricular
Medical specialty
Neurology
Review panel
Neurology
Device class
2
Clearance type
Special
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
JOYCE KILROY
Address
3773 Corporate Pkwy. Center Valley PA US 18034 18034

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

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