Model 1051, Monitor

FDA 510(k) K790328 · Applied Medical Research

Substantially Equivalent

510(k) numberK790328

Submission

Device name
Model 1051, Monitor
Applicant
Applied Medical Research
Mchenry, IL, US
Received
February 16, 1979
Decision date
March 2, 1979
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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More from 80 Beats Medical GmbH

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K800025Dinamap Research Monitor 1245DXN · Traditional 02/01/1980SE
K791580Cerebral Function Monitor 870OMA · Traditional 09/04/1979SE
K791159Dinamap Model 855DXN · Traditional 07/30/1979SE
K790322Optional Accessory Foot Switch Model 100EBW · Traditional 05/14/1979SE
K782073Dinamap Models 1160 and 1165DSK · Traditional 02/23/1979SE
K781064Dinamap Model 848DSK · Traditional 09/07/1978SE
K781053Dinamap Model 846DSK · Traditional 09/07/1978SE
K781311Electrode, Needle, CFMGXZ · Traditional 08/21/1978SE
K780754Neonatal MonitorDXN · Traditional 06/14/1978SE
K780759Model 902 StandFSH · Traditional 05/19/1978SE

Questions and answers

When was Model 1051, Monitor cleared by the FDA?

Model 1051, Monitor (K790328) received a 510(k) decision of Substantially Equivalent on March 2, 1979, 14 days after the submission was received.

What is the product code of K790328?

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