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FDA 510(k)

SARA AGIE MONITOR

K-Number: K874724 · 1988-03-29

ApplicantPpg/Applied Resources, Inc.
Decision Date1988-03-29
Product CodeCCK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SARA AGIE MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Ppg/Applied Resources, Inc.. It received FDA 510(k) clearance on 1988-03-29 under 510(k) number K874724. 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 SARA AGIE MONITOR?

SARA AGIE MONITOR is a medical device that received FDA 510(k) clearance on 1988-03-29. The listed applicant is Ppg/Applied Resources, Inc.. The 510(k) number is K874724.

When did SARA AGIE MONITOR receive FDA 510(k) clearance?

SARA AGIE MONITOR received FDA 510(k) clearance on 1988-03-29, under 510(k) number K874724.

Who is the listed applicant for SARA AGIE MONITOR?

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

What is the FDA product code for SARA AGIE MONITOR?

The FDA product code for SARA AGIE MONITOR 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 Ppg/Applied Resources, 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.

K881002O.R. SARACAPK881093ICU SARACAPK882172SARACAP AGK874754SARA DIGICAP

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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