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FDA 510(k)

MASS SPECTROMETRY MONITORING LINES AND CONNECTORS

K-Number: K900291 · 1990-03-28

ApplicantF.L.W. Plastics, Inc.
Decision Date1990-03-28
Product CodeCCK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MASS SPECTROMETRY MONITORING LINES AND CONNECTORS is the device name listed in this FDA 510(k) record. The listed applicant is F.L.W. Plastics, Inc.. It received FDA 510(k) clearance on 1990-03-28 under 510(k) number K900291. 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 MASS SPECTROMETRY MONITORING LINES AND CONNECTORS?

MASS SPECTROMETRY MONITORING LINES AND CONNECTORS is a medical device that received FDA 510(k) clearance on 1990-03-28. The listed applicant is F.L.W. Plastics, Inc.. The 510(k) number is K900291.

When did MASS SPECTROMETRY MONITORING LINES AND CONNECTORS receive FDA 510(k) clearance?

MASS SPECTROMETRY MONITORING LINES AND CONNECTORS received FDA 510(k) clearance on 1990-03-28, under 510(k) number K900291.

Who is the listed applicant for MASS SPECTROMETRY MONITORING LINES AND CONNECTORS?

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

What is the FDA product code for MASS SPECTROMETRY MONITORING LINES AND CONNECTORS?

The FDA product code for MASS SPECTROMETRY MONITORING LINES AND CONNECTORS is CCK.

Related Clinical Trials

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Other records listing F.L.W. Plastics, Inc. 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.

K895233BACTERIAL AND VIRAL FILTERK895357ANETHESIA BREATHING CIRCUITK895169MANUAL DISPOSABLE PULMONARY RESUSCITATOR

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

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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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