Technicuff

510(k) Number

K942259 ↗

FDA product code

DXQ

Device class

Class II

Regulation

21 CFR Part 870.1120

Advisory committee

Cardiovascular

FDA decision

SESE Substantially Equivalent

Clearances this device's FDA summary refers to, and clearances whose summaries refer to it: a citation, not a claim of equivalence.

Source: 510k-lineage (choiben314), CC BY 4.0

Devices that FDA's GUDID lists as cleared or approved under this submission number. One submission usually covers a whole product family, so the sizes and models are listed here once.

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

• MINIMUS II; MINIMUS II COLOR; BABYPHON by Rudolf Riester GmbH & Co. KG
• OCL CONTOUR by M-Pact Worldwide, LLC
• Welch Allyn, Inc. 901041 DS44 by Welch Allyn, Inc.
• ONE-CUF by GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES, INC.
• CUFF, BLOOD PRESSURE by Buffalo Medical Specialties Mfg., Inc.
• Welch Allyn, Inc. 901041 DS45 by Welch Allyn, Inc.
• NIBP Neo #1 Cuff 3.1 - 5.7 cm 2870181 by Draeger Medical Systems, Inc.
• Value Care Cuff Large Adult, Value Care Cuff Adult XL (extra long), Value Care Cuff Adult, Value Care Cuff Small Adult, Value Care Cuff Pediatric, Value Care Cuff Infant, Efficia Adult NIBP Airhose, 3 M, Efficia Adult NIBP Air Hose, 1.5 M by Philips Medical Systems
• Medline Reusable Blood Pressure Cuff by MEDLINE INDUSTRIES, INC.
• CYPRESS MEDICAL PRODUCTS ANEROID SPHYGMOMANOMETER by Cypress Medical Products, Ltd.

• Technicuff UT-3962L

  Class II

  FDA 510(k) K942259 Active Cleared 6 Sep 1994 GUDID on market

• Technicuff UP-0925

  Class II

  FDA 510(k) K942259 Active Cleared 6 Sep 1994 GUDID on market

• Technicuff UA-1745L

  Class II

  FDA 510(k) K942259 Active Cleared 6 Sep 1994 GUDID on market

• Technicuff UN-0309

  Class II

  FDA 510(k) K942259 Active Cleared 6 Sep 1994 GUDID on market

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