Rossmax Medipro Model 10 and 60, Medicare Model 10 and 60 Blood Pressure Monitors

No FDA recalls found in the data synced 22 Oct 2026.

510(k) Number

K013583 ↗

FDA Product Code

DXN

Models / Variants

10

60

Medicare Model 10

60 Blood Pressure Monitors

FDA applicant

Rossmax International , Ltd.

Device Class

Class II

Regulation

21 CFR Part 870.1130

Advisory Committee

Cardiovascular

FDA Decision

SESE Substantially Equivalent

• Rossmax Automatic Wristwatch Blood Pressure Monitor, Model Rm-4100

  Class II

  FDA 510(k) K992387 Active Cleared 3 Aug 1999

• Rossmax Automatic Wristwatch Blood Pressure Monitor, Model V46

  Class II

  FDA 510(k) K993542 Active Cleared 29 Dec 1999

• Rossmax Non-Invasive Blood Pressure Monitors, Models S380, K350

  Class II

  FDA 510(k) K052727 Active Cleared 16 Dec 2005

• Rossmax Automatic Wristwatch Blood Pressure Monitor, Model BPW138

  Class II

  FDA 510(k) K011523 Active Cleared 14 Jun 2001

• Rossmax Automatic Wristwatch Blood Pressure Monitor, Model Z46

  Class II

  FDA 510(k) K993432 Active Cleared 20 Dec 1999

• Rossmax Automatic Wristwatch Blood Pressure Monitor, Model Rm-4000

  Class II

  FDA 510(k) K964153 Active Cleared 11 Jun 1998

See all devices from Rossmax International, Ltd. →