Digital Blood Pressure Unit

FDA 510(k) K813385 · Conphar, Inc.

Substantially Equivalent

510(k) numberK813385

Submission

Device name
Digital Blood Pressure Unit
Applicant
Conphar, Inc.
Walker, MI, US
Received
December 2, 1981
Decision date
January 29, 1982
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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Questions and answers

When was Digital Blood Pressure Unit cleared by the FDA?

Digital Blood Pressure Unit (K813385) received a 510(k) decision of Substantially Equivalent on January 29, 1982, 58 days after the submission was received.

What is the product code of K813385?

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