Acu-Guard 0ADG51

• FDA 510(k) K915000 decided 27 Jan 1992 Active
• FDA GUDID UDI-DI 00814105020852 listed 3 Jan 2020 Listed

1. 27 Jan 1992 Cleared FDA 510(k) K915000
2. 3 Jan 2020 Listed FDA GUDID 00814105020852

Trade name

Acu-Guard

Generic name

Medical equipment drape, single-use, non-sterile

Model / reference

0ADG51

Primary DI / UDI-DI

00814105020852

510(k) Number

K915000 ↗

FDA product code

GEX

GMDN term

Medical equipment drape, single-use, non-sterile

Device class

Class II

Regulation number

878.4810

GUDID distribution status

In Commercial Distribution

Category: Medical equipment drape, single-use, non-sterile

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See all devices from Acuderm, Inc. →