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FDA 510(k)

MODEL 7000 COMBINATION END TIDAL & PULSE OXIMETRY

K-Number: K874036 · 1987-11-06

ApplicantNovametrix Medical Systems, Inc.
Decision Date1987-11-06
Product CodeCCK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MODEL 7000 COMBINATION END TIDAL & PULSE OXIMETRY 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 1987-11-06 under 510(k) number K874036. 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 MODEL 7000 COMBINATION END TIDAL & PULSE OXIMETRY?

MODEL 7000 COMBINATION END TIDAL & PULSE OXIMETRY is a medical device that received FDA 510(k) clearance on 1987-11-06. The listed applicant is Novametrix Medical Systems, Inc.. The 510(k) number is K874036.

When did MODEL 7000 COMBINATION END TIDAL & PULSE OXIMETRY receive FDA 510(k) clearance?

MODEL 7000 COMBINATION END TIDAL & PULSE OXIMETRY received FDA 510(k) clearance on 1987-11-06, under 510(k) number K874036.

Who is the listed applicant for MODEL 7000 COMBINATION END TIDAL & PULSE OXIMETRY?

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 MODEL 7000 COMBINATION END TIDAL & PULSE OXIMETRY?

The FDA product code for MODEL 7000 COMBINATION END TIDAL & PULSE OXIMETRY 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

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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