510(k) K940970

Device
YASARGIL, CASPAR, VARIO CLIP APPLIERS
Applicant
Aesculap, Inc.
510(k) number
K940970
Product code
HCI
Decision
Substantially Equivalent (SESE)
Decision date
1995-01-24
Date received
1994-03-02
Regulation
882.4175
Classification name
Applier, Aneurysm Clip
Medical specialty
Neurology
Review panel
Neurology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N
Source
FDA openFDA 510(k) dataset plus migrated FDA.report data

Related Records

Applicant Contact

Contact
VISTORIA MACKINNON
Address
1000 Gateway Blvd. South San Francisco CA US 94080 94080

FDA Registration Numbers

Source Documents

FDA 510(k) Premarket Notification Database · 510(k) summary PDF · openFDA JSON

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