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FDA 510(k)

TMM MODEL 2500 CAPMONITOR

K-Number: K875268 · 1988-01-22

ApplicantTraverse Medical Monitors
Decision Date1988-01-22
Product CodeCCK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

TMM MODEL 2500 CAPMONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Traverse Medical Monitors. It received FDA 510(k) clearance on 1988-01-22 under 510(k) number K875268. 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 TMM MODEL 2500 CAPMONITOR?

TMM MODEL 2500 CAPMONITOR is a medical device that received FDA 510(k) clearance on 1988-01-22. The listed applicant is Traverse Medical Monitors. The 510(k) number is K875268.

When did TMM MODEL 2500 CAPMONITOR receive FDA 510(k) clearance?

TMM MODEL 2500 CAPMONITOR received FDA 510(k) clearance on 1988-01-22, under 510(k) number K875268.

Who is the listed applicant for TMM MODEL 2500 CAPMONITOR?

The FDA 510(k) record lists Traverse Medical Monitors as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TMM MODEL 2500 CAPMONITOR?

The FDA product code for TMM MODEL 2500 CAPMONITOR is CCK.

Related Clinical Trials

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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Other records listing Traverse Medical Monitors as applicant

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.

K863801TMM MODEL 3000 ANESTHESIA CIRCUIT EVALUATOR

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.

K251641GF-310R Multigas Unit (GF-310R)Nihon Kohden CorporationK261633VisuBreathAffirm Medical Technologies II, LLCK253030Capnostream™35 Portable Respiratory Monitor (PM35MN)Covidien, LLCK250148Medical Gas Analyzer (AG200)Prior Care Science Technology, Ltd.K243956TG-980P CO2 Sensor Kit (TG-980P); TG-980P1 CO2 Sensor Kit (TG-980P1)Nihon Kohden CorporationK2512160184 CO2 Sampling line; 0184T CO2 Sampling line; 0139 CO2 Sampling line; 0182 CO2 Sampling lineBarbaras Development, Inc.

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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