All Purpose Cuff 98-0082-09

• FDA 510(k) K051904 decided 9 Sep 2005 Active
• FDA GUDID UDI-DI 10840935101444 listed 12 Sep 2016 Listed

1. 9 Sep 2005 Cleared FDA 510(k) K051904
2. 12 Sep 2016 Listed FDA GUDID 10840935101444

Trade name

All Purpose Cuff

Generic name

Blood pressure cuff, reusable

Model / reference

98-0082-09

Primary DI / UDI-DI

10840935101444

510(k) Number

K051904 ↗

FDA product code

DXQ

GMDN term

Blood pressure cuff, reusable

Device class

Class II

Regulation number

870.1120

GUDID distribution status

In Commercial Distribution

Category: Blood pressure cuff, reusable

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

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• CAMOUFLAGE CUFF SAVERS by N.A. Braggs Medical, Inc.
• MDF® MDF840D14 by MDF Instruments Medifriend Inc.
• MEDIFRIEND PROFESSIONAL SPHYGMOMANOMETER by Shanghai Medifriend Medical Products Co., Ltd.
• ETHOX SURGI-CUF ADULT DISPOSABLE BLOOD PRESSURE CUFFS by Ethox Corp.
• PROTECT ALL BLOOD PRESSURE CUFF COVER by Protect All, Inc.
• NEONATAL BLOOD PRESSURE CUFF by Invivo Research, Inc.
• ANEROID SPHYGMOMETER by Swartz Medical Equipment
• ANEROID TYPE BLOOD PRESSURE KIT by Mars Metal Co., Ltd.
• SAMA DISPOSABLE BLOOD PRESSURE CUFF BARRIERS by Pinhu Sama Medical Packing Co., Ltd.

• LPXpod Pulse Oximeter Cable

  Class IIa

  CE/MDR

• SunTech SpO2 Module

  Class IIa

  CE/MDR

• Patient Hose 91-0028-23

  Class II

  FDA 510(k) K051904 Active Cleared 9 Sep 2005 GUDID on market

• Straight Black Hose, Female Bayonet to Female Bayonet, 9.8ft (3m), Siemens 91-0032-33

  Class II

  FDA 510(k) K051904 Active Cleared 9 Sep 2005 GUDID on market

See all devices from SunTech Medical, Inc →