Vector R&D, Inc VKS6W

• FDA 510(k) K051872 decided 3 Oct 2005 Active
• FDA GUDID UDI-DI 00810113690209 listed 30 Sep 2022 Listed

1. 3 Oct 2005 Cleared FDA 510(k) K051872
2. 30 Sep 2022 Listed FDA GUDID 00810113690209

Trade name

Vector R&D, Inc

Generic name

Pneumatic dental handpiece coupler

Model / Ref / Catalog

VKS6W

Primary DI / UDI-DI

00810113690209

510(k) Number

K051872 ↗

FDA product code

EFB

GMDN term

Pneumatic dental handpiece coupler

Device class

Class I

Regulation number

872.4200

GUDID distribution status

In Commercial Distribution

MRI safety

MR Unsafe

Category: Pneumatic dental handpiece coupler

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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. →