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FDA 510(k)

CAPNOMETER

K-Number: K842325 · 1984-06-26

ApplicantSensors, Inc.
Decision Date1984-06-26
Product CodeCCK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CAPNOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Sensors, Inc.. It received FDA 510(k) clearance on 1984-06-26 under 510(k) number K842325. 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 CAPNOMETER?

CAPNOMETER is a medical device that received FDA 510(k) clearance on 1984-06-26. The listed applicant is Sensors, Inc.. The 510(k) number is K842325.

When did CAPNOMETER receive FDA 510(k) clearance?

CAPNOMETER received FDA 510(k) clearance on 1984-06-26, under 510(k) number K842325.

Who is the listed applicant for CAPNOMETER?

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

What is the FDA product code for CAPNOMETER?

The FDA product code for CAPNOMETER is CCK.

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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

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

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