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FDA 510(k)

KONTRON MINIMON 7131 PATIENT MONITOR

K-Number: K844733 · 1985-03-27

ApplicantKontron Instruments, Inc.
Decision Date1985-03-27
Product CodeDRT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

KONTRON MINIMON 7131 PATIENT MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Kontron Instruments, Inc.. It received FDA 510(k) clearance on 1985-03-27 under 510(k) number K844733. The device is classified under product code DRT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KONTRON MINIMON 7131 PATIENT MONITOR?

KONTRON MINIMON 7131 PATIENT MONITOR is a medical device that received FDA 510(k) clearance on 1985-03-27. The listed applicant is Kontron Instruments, Inc.. The 510(k) number is K844733.

When did KONTRON MINIMON 7131 PATIENT MONITOR receive FDA 510(k) clearance?

KONTRON MINIMON 7131 PATIENT MONITOR received FDA 510(k) clearance on 1985-03-27, under 510(k) number K844733.

Who is the listed applicant for KONTRON MINIMON 7131 PATIENT MONITOR?

The FDA 510(k) record lists Kontron Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KONTRON MINIMON 7131 PATIENT MONITOR?

The FDA product code for KONTRON MINIMON 7131 PATIENT MONITOR is DRT.

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Other records listing Kontron Instruments, Inc. as applicant

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Related Devices (Code: DRT)

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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