SoftCheck ST2938FL

• FDA 510(k) K940214 decided 22 Feb 1994 Active
• FDA GUDID UDI-DI 00858293006595 listed 30 Aug 2019 Listed

1. 22 Feb 1994 Cleared FDA 510(k) K940214
2. 30 Aug 2019 Listed FDA GUDID 00858293006595

Trade name

SoftCheck

Generic name

Blood pressure cuff, single-use

Model / reference

ST2938FL

Primary DI / UDI-DI

00858293006595

510(k) Number

K940214 ↗

FDA product code

DXQ

GMDN term

Blood pressure cuff, single-use

Device class

Class II

Regulation number

870.1120

GUDID distribution status

In Commercial Distribution

Category: Blood pressure cuff, single-use

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

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• Welch Allyn, Inc. 901040 7670-01S by Welch Allyn, Inc.
• CYPRESS MEDICAL PRODUCTS ANEROID SPHYGMOMANOMETER by Cypress Medical Products, Ltd.
• CAREMATE SPHYGMOMANOMETER WITH STETHOSCOPE by CAREMATE MEDICAL DEVICE CO., LTD
• NIBP Neo #2 Cuff 4.3 - 8 cm 2870199 by Draeger Medical Systems, Inc.
• SENSA-CUFF, MODELS INFANT, CHILD, ADULT by GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES, INC.
• Aneroid Type Blood Pressure Kit by Dongguan Mars Medical Products Co., Ltd.
• BLOOD PRESSURE SLEEVE W/TUBING by Devcom, Inc.
• ULTRACHECK SPACELABS ABP CUFF-CHILD, ULTRACHECK SPACELABS ABP CUFF-SMALL ADULT, ULTRACHECK SPACELABS ABP CUFF-ADULT, ULTRACHECK SPACELABS ABP CUFF-LARGE ADULT by Statcorp Medical
• NORELCO ANEROID BLOOD PRESSURE METER by North American Philips Corp.

• Peracidin 081896

  Class II

  FDA 510(k) K962959 Active Cleared 5 Jun 1998 GUDID on market

• Peracidin 081894

  Class II

  FDA 510(k) K962959 Active Cleared 5 Jun 1998 GUDID on market

• EZ-Chek K100-0111

  Class II

  FDA 510(k) K132344 Active Cleared 25 Feb 2014 GUDID on market

• Spiral Coil Tubing, Trans Blue 1W-025-27

  Class I

  GUDID on market

See all devices from Reprocessing Products Corp →