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FDA 510(k)

SARACAP RESPIRATORY MONITOR

K-Number: K852062 · 1985-08-06

ApplicantAlleghany Intl. Medical Technology
Decision Date1985-08-06
Product CodeCCK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SARACAP RESPIRATORY MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Alleghany Intl. Medical Technology. It received FDA 510(k) clearance on 1985-08-06 under 510(k) number K852062. 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 SARACAP RESPIRATORY MONITOR?

SARACAP RESPIRATORY MONITOR is a medical device that received FDA 510(k) clearance on 1985-08-06. The listed applicant is Alleghany Intl. Medical Technology. The 510(k) number is K852062.

When did SARACAP RESPIRATORY MONITOR receive FDA 510(k) clearance?

SARACAP RESPIRATORY MONITOR received FDA 510(k) clearance on 1985-08-06, under 510(k) number K852062.

Who is the listed applicant for SARACAP RESPIRATORY MONITOR?

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

What is the FDA product code for SARACAP RESPIRATORY MONITOR?

The FDA product code for SARACAP RESPIRATORY 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 Alleghany Intl. Medical Technology 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.

K862880SARA RTK861398PRE-CHECK C02 DETECTOR

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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