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FDA 510(k)

KONTRON CAPNOGRAPH MONITOR, SUPERMON MODULE 7281

K-Number: K873396 · 1988-06-21

ApplicantKontron Instruments, Inc.
Decision Date1988-06-21
Product CodeCCK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

KONTRON CAPNOGRAPH MONITOR, SUPERMON MODULE 7281 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 1988-06-21 under 510(k) number K873396. The device is classified under product code CCK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KONTRON CAPNOGRAPH MONITOR, SUPERMON MODULE 7281?

KONTRON CAPNOGRAPH MONITOR, SUPERMON MODULE 7281 is a medical device that received FDA 510(k) clearance on 1988-06-21. The listed applicant is Kontron Instruments, Inc.. The 510(k) number is K873396.

When did KONTRON CAPNOGRAPH MONITOR, SUPERMON MODULE 7281 receive FDA 510(k) clearance?

KONTRON CAPNOGRAPH MONITOR, SUPERMON MODULE 7281 received FDA 510(k) clearance on 1988-06-21, under 510(k) number K873396.

Who is the listed applicant for KONTRON CAPNOGRAPH MONITOR, SUPERMON MODULE 7281?

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 CAPNOGRAPH MONITOR, SUPERMON MODULE 7281?

The FDA product code for KONTRON CAPNOGRAPH MONITOR, SUPERMON MODULE 7281 is CCK.

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Other records listing Kontron Instruments, Inc. as applicant

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Related Devices (Code: CCK)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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