Cannula Standard

• FDA 510(k) K120098 decided 12 Jun 2012 Active
• FDA GUDID UDI-DI 07290014954717 listed 24 Sep 2016 Listed

1. 12 Jun 2012 Cleared FDA 510(k) K120098
2. 24 Sep 2016 Listed FDA GUDID 07290014954717

Trade name

Cannula

Generic name

Intracerebral cannula, implantable

Model / Ref / Catalog

Standard, STR-000087-31

Primary DI / UDI-DI

07290014954717

510(k) Number

K120098 ↗

FDA product code

GZL

GMDN term

Intracerebral cannula, implantable

Device class

Class II

Regulation number

882.1330

GUDID distribution status

In Commercial Distribution

MRI safety

MR Unsafe

Category: Intracerebral cannula, implantable

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See all devices from Alpha Omega Engineering Corp. →