ASA Techmed AS-MC-PED

• FDA 510(k) K082542 decided 17 Sep 2008 Active
• FDA GUDID UDI-DI 06970366970030 listed 4 Dec 2018 Listed

1. 17 Sep 2008 Cleared FDA 510(k) K082542
2. 4 Dec 2018 Listed FDA GUDID 06970366970030

Trade name

ASA Techmed

Generic name

Aneroid manual sphygmomanometer

Model / reference

AS-MC-PED

Primary DI / UDI-DI

06970366970030

510(k) Number

K082542 ↗

FDA product code

DXQ

GMDN term

Aneroid manual sphygmomanometer

Device class

Class II

Regulation number

870.1120

GUDID distribution status

In Commercial Distribution

Category: Aneroid manual sphygmomanometer

Other devices filed under FDA product code DXQ (Blood Pressure Cuff).

• NEONATAL/STERILE/DISPOS/NONINVAS BLOOD PRESS CUFF by Hewlett-Packard Co.
• WELCH ALLYN DURASHOCK BLOOD PRESSURE SYSTEM by Welch Allyn, Inc.
• MDF® MDF83004 by MDF Instruments Medifriend Inc.
• Welch Allyn FlexiPort Blood Pressure Cuffs (FlexiPort Blood Pressure Cuffs) by Baxter Healthcare Corp
• ANEROID AND MERCURIAL SPHYGMOMANOMETERS by American Diagnostic Corporation
• POLYURETHANE BLOOD PRESSURE CUFFS by D. E. Hokanson, Inc.
• CUF-COVER (TM) by Ethox Corp.
• ANEROID SPHYGMOMANOMETER, DOCTOR TYPE by Yamasu Co., Ltd.
• Reusable Blood Pressure Cuff, Disposable Blood Pressure Cuff by Ningbo Albert Novosino Co.,Ltd.
• Disposable Blood Pressure Cuff by Wenzhou Xikang Medical Instruments Co., Ltd.

• ASA Techmed AS-MC

  Class II

  FDA 510(k) K082542 Active Cleared 17 Sep 2008 GUDID on market

• As-P65

  Class II

  FDA 510(k) K082542 Active Cleared 17 Sep 2008 GUDID on market

• None As-Nd

  Class II

  FDA 510(k) K082542 Active Cleared 17 Sep 2008 GUDID on market

• ASA Techmed AS-MC-TH

  Class II

  FDA 510(k) K082542 Active Cleared 17 Sep 2008 GUDID on market

See all devices from Cardicare Company Ltd →