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FDA 510(k)

SUPERMON NEONATAL NON-INVASIVE BLOOD PRESS. 7283

K-Number: K882955 · 1990-01-26

ApplicantKontron Instruments, Inc.
Decision Date1990-01-26
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SUPERMON NEONATAL NON-INVASIVE BLOOD PRESS. 7283 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 1990-01-26 under 510(k) number K882955. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUPERMON NEONATAL NON-INVASIVE BLOOD PRESS. 7283?

SUPERMON NEONATAL NON-INVASIVE BLOOD PRESS. 7283 is a medical device that received FDA 510(k) clearance on 1990-01-26. The listed applicant is Kontron Instruments, Inc.. The 510(k) number is K882955.

When did SUPERMON NEONATAL NON-INVASIVE BLOOD PRESS. 7283 receive FDA 510(k) clearance?

SUPERMON NEONATAL NON-INVASIVE BLOOD PRESS. 7283 received FDA 510(k) clearance on 1990-01-26, under 510(k) number K882955.

Who is the listed applicant for SUPERMON NEONATAL NON-INVASIVE BLOOD PRESS. 7283?

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 SUPERMON NEONATAL NON-INVASIVE BLOOD PRESS. 7283?

The FDA product code for SUPERMON NEONATAL NON-INVASIVE BLOOD PRESS. 7283 is DXN.

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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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