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FDA 510(k)

NOVAMETRIX MODEL 1265 END TIDAL CARBON DIOXIDE MON

K-Number: K910019 · 1991-03-26

ApplicantNovametrix Medical Systems, Inc.
Decision Date1991-03-26
Product CodeCCK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

NOVAMETRIX MODEL 1265 END TIDAL CARBON DIOXIDE MON is the device name listed in this FDA 510(k) record. The listed applicant is Novametrix Medical Systems, Inc.. It received FDA 510(k) clearance on 1991-03-26 under 510(k) number K910019. 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 NOVAMETRIX MODEL 1265 END TIDAL CARBON DIOXIDE MON?

NOVAMETRIX MODEL 1265 END TIDAL CARBON DIOXIDE MON is a medical device that received FDA 510(k) clearance on 1991-03-26. The listed applicant is Novametrix Medical Systems, Inc.. The 510(k) number is K910019.

When did NOVAMETRIX MODEL 1265 END TIDAL CARBON DIOXIDE MON receive FDA 510(k) clearance?

NOVAMETRIX MODEL 1265 END TIDAL CARBON DIOXIDE MON received FDA 510(k) clearance on 1991-03-26, under 510(k) number K910019.

Who is the listed applicant for NOVAMETRIX MODEL 1265 END TIDAL CARBON DIOXIDE MON?

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

What is the FDA product code for NOVAMETRIX MODEL 1265 END TIDAL CARBON DIOXIDE MON?

The FDA product code for NOVAMETRIX MODEL 1265 END TIDAL CARBON DIOXIDE MON is CCK.

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Related Devices (Code: CCK)

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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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