Baro/Trac II & Vita/Trac, Vital Sign Mon

FDA 510(k) K801389 · Bib, Inc.

Substantially Equivalent

510(k) numberK801389

Submission

Device name
Baro/Trac II & Vita/Trac, Vital Sign Mon
Applicant
Bib, Inc.
Mchenry, IL, US
Received
June 13, 1980
Decision date
July 28, 1980
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
DXN – System, Measurement, Blood-Pressure, Non-Invasive
Device class
Class II (moderate risk)
Regulation
21 CFR 870.1130
Specialty
Cardiovascular

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K261394Arm-type Fully Automatic Digital Blood Pressure Monitor (DBP-6186 Plus, DBP-6286B Plus…DXN · Traditional JOYTECH Healthcare Co., Ltd.08/26/2026SE
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K253425Arm-type Fully Automatic Digital Blood Pressure Monitor…DXN · Traditional Joytech Healthcare Co. , Ltd.08/13/2026SE
K261136Blood Pressure Monitor (M501,M501A,M502,M502A,M502C,M502D)DXN · Traditional Guangzhou Daxin Health Technology Co., Ltd.07/23/2026SE
K261082Microlife Wrist Blood Pressure Monitor , (Model BPHJG5-G)DXN · Traditional Microlife Corporation07/23/2026SE
K253126Wrist Blood Pressure Monitor (XW-05)DXN · Traditional Shenzhen Ziqing Medical Equipment Co., Ltd.06/18/2026SE
K260693VicorderCS (VCS-SYS-1100)DXN · Traditional 80 Beats Medical GmbH06/16/2026SE

More from 80 Beats Medical GmbH

510(k)DeviceDecision
K830916Vita/Trac 4 Function Vital Sign MonitorDRT · Traditional 07/07/1983SE
K801366Disposable Temperature Probe CoverFLL · Traditional 07/28/1980SE
K800596Vita/Trac 4-FUNCTION Vital Sign MonitorDXN · Traditional 07/21/1980SE
K800782Pace-Pulse/ComputracKRE · Traditional 05/28/1980SE

Questions and answers

When was Baro/Trac II & Vita/Trac, Vital Sign Mon cleared by the FDA?

Baro/Trac II & Vita/Trac, Vital Sign Mon (K801389) received a 510(k) decision of Substantially Equivalent on July 28, 1980, 45 days after the submission was received.

What is the product code of K801389?

The FDA product code is DXN – System, Measurement, Blood-Pressure, Non-Invasive, a Class II (moderate risk) device regulated under 21 CFR 870.1130.