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FDA 510(k)

KONTRON SUPERMON CARDIAC OUTPUT MODULE 7263

K-Number: K862261 · 1987-02-19

ApplicantKontron Instruments, Inc.
Decision Date1987-02-19
Product CodeDXG
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

KONTRON SUPERMON CARDIAC OUTPUT MODULE 7263 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 1987-02-19 under 510(k) number K862261. The device is classified under product code DXG. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KONTRON SUPERMON CARDIAC OUTPUT MODULE 7263?

KONTRON SUPERMON CARDIAC OUTPUT MODULE 7263 is a medical device that received FDA 510(k) clearance on 1987-02-19. The listed applicant is Kontron Instruments, Inc.. The 510(k) number is K862261.

When did KONTRON SUPERMON CARDIAC OUTPUT MODULE 7263 receive FDA 510(k) clearance?

KONTRON SUPERMON CARDIAC OUTPUT MODULE 7263 received FDA 510(k) clearance on 1987-02-19, under 510(k) number K862261.

Who is the listed applicant for KONTRON SUPERMON CARDIAC OUTPUT MODULE 7263?

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 SUPERMON CARDIAC OUTPUT MODULE 7263?

The FDA product code for KONTRON SUPERMON CARDIAC OUTPUT MODULE 7263 is DXG.

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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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