VECTORVISION CRANIAL, VECTORVISION ENT, KOLIBRI CRANIAL, KOLIBRI ENT, CRANIAL ESSENTIAL, CRANIAL UNLIMITED

FDA 510(k) Premarket Notification · Submission K092467 · Applicant: Brainlab AG

Public Record 510(k) Submission Decision Date: 2010-05-06 510(k) record compiled from public FDA source records.

Submission Details & Decision

Normalized public record details for 510(k) notification K092467.

Source Dataset
FDA 510(k) Premarket Notifications
510(k) Number
K092467
Applicant / Sponsor
Device Name
VECTORVISION CRANIAL, VECTORVISION ENT, KOLIBRI CRANIAL, KOLIBRI ENT, CRANIAL ESSENTIAL, CRANIAL UNLIMITED
Product Code
HAW
Decision Date
2010-05-06
Decision / Status
Substantially Equivalent (SESE)
Advisory Committee
Neurology (NE)
Clearance Type
Special
Third Party Flag
N
Date Received
2009-08-12

Related Establishments / Registrations

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