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FDA 510(k)

SUPERMON NON-INVASIVE BLOOD PRESSURE MODULE 7282

K-Number: K861374 · 1987-07-21

ApplicantKontron Instruments, Inc.
Decision Date1987-07-21
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SUPERMON NON-INVASIVE BLOOD PRESSURE MODULE 7282 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 1987-07-21 under 510(k) number K861374. 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 NON-INVASIVE BLOOD PRESSURE MODULE 7282?

SUPERMON NON-INVASIVE BLOOD PRESSURE MODULE 7282 is a medical device that received FDA 510(k) clearance on 1987-07-21. The listed applicant is Kontron Instruments, Inc.. The 510(k) number is K861374.

When did SUPERMON NON-INVASIVE BLOOD PRESSURE MODULE 7282 receive FDA 510(k) clearance?

SUPERMON NON-INVASIVE BLOOD PRESSURE MODULE 7282 received FDA 510(k) clearance on 1987-07-21, under 510(k) number K861374.

Who is the listed applicant for SUPERMON NON-INVASIVE BLOOD PRESSURE MODULE 7282?

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 NON-INVASIVE BLOOD PRESSURE MODULE 7282?

The FDA product code for SUPERMON NON-INVASIVE BLOOD PRESSURE MODULE 7282 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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