Electronic Blood Pressure Unit

FDA 510(k) K761302 · Medline Industries, Inc.

Substantially Equivalent

510(k) numberK761302

Submission

Device name
Electronic Blood Pressure Unit
Applicant
Medline Industries, Inc.
Mchenry, IL, US
Received
December 11, 1976
Decision date
January 5, 1977
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 Electronic Blood Pressure Unit cleared by the FDA?

Electronic Blood Pressure Unit (K761302) received a 510(k) decision of Substantially Equivalent on January 5, 1977, 25 days after the submission was received.

What is the product code of K761302?

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