Biochem 6100 Non-Invasive Monitor

FDA 510(k) K903222 · Biochem International, Inc.

Substantially Equivalent

510(k) numberK903222

Submission

Device name
Biochem 6100 Non-Invasive Monitor
Applicant
Biochem International, Inc.
Waukesha, WI, US
Received
July 23, 1990
Decision date
September 4, 1990
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 Biochem 6100 Non-Invasive Monitor cleared by the FDA?

Biochem 6100 Non-Invasive Monitor (K903222) received a 510(k) decision of Substantially Equivalent on September 4, 1990, 43 days after the submission was received.

What is the product code of K903222?

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