Medtek #411 Portable B-P Instr.

FDA 510(k) K800614 · Med-Tek Corp.

Substantially Equivalent

510(k) numberK800614

Submission

Device name
Medtek #411 Portable B-P Instr.
Applicant
Med-Tek Corp.
Mchenry, IL, US
Received
March 18, 1980
Decision date
April 2, 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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Questions and answers

When was Medtek #411 Portable B-P Instr. cleared by the FDA?

Medtek #411 Portable B-P Instr. (K800614) received a 510(k) decision of Substantially Equivalent on April 2, 1980, 15 days after the submission was received.

What is the product code of K800614?

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