Vector R&D, Inc GT-XTC

• FDA 510(k) K070155 decided 25 Jan 2007 Active
• FDA GUDID UDI-DI 00810113691008 listed 30 Sep 2022 Listed

1. 25 Jan 2007 Cleared FDA 510(k) K070155
2. 30 Sep 2022 Listed FDA GUDID 00810113691008

Trade name

Vector R&D, Inc

Generic name

Dental delivery system instrument unit, pneumatic

Model / Ref / Catalog

GT-XTC

Primary DI / UDI-DI

00810113691008

510(k) Number

K070155 ↗

FDA product code

EFB

GMDN term

Dental delivery system instrument unit, pneumatic

Device class

Class I

Regulation number

872.4200

GUDID distribution status

In Commercial Distribution

MRI safety

MR Unsafe

Category: Dental delivery system instrument unit, pneumatic

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• Vector R&D, Inc DRA-NK

  Class I

  FDA 510(k) K051872 Active Cleared 3 Oct 2005 GUDID on market

• Vector R&D, Inc F4

  Class I

  FDA 510(k) K032234 Active Cleared 2 Oct 2003 GUDID on market

• Vector R&D, Inc VM25LPA

  Class I

  FDA 510(k) K051872 Active Cleared 3 Oct 2005 GUDID on market

• Vector R&D, Inc KV80

  Class I

  FDA 510(k) K051872 Active Cleared 3 Oct 2005 GUDID on market

See all devices from Vector R&D, Inc. →