Reusable Frame, Best Precision Stepper 6050

• FDA 510(k) K973786 decided 2 Jan 1998 Active
• FDA GUDID UDI-DI 00852656007175 listed 31 Oct 2016 Listed

1. 2 Jan 1998 Cleared FDA 510(k) K973786
2. 31 Oct 2016 Listed FDA GUDID 00852656007175

Trade name

Reusable Frame, Best Precision Stepper

Generic name

Needle guide, reusable

Model / reference

6050

Primary DI / UDI-DI

00852656007175

510(k) Number

K973786 ↗

FDA product code

IWJ

GMDN term

Needle guide, reusable

Device class

Class I

Regulation number

892.5650

GUDID distribution status

In Commercial Distribution

Sterilisation method

Moist Heat or Steam Sterilization

Category: Needle guide, reusable

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See all devices from Best Nomos →