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FDA 510(k)

700/700-1

K-Number: K924083 · 1993-03-10

ApplicantCiticare Systems, Inc.
Decision Date1993-03-10
Product CodeCCK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

700/700-1 is the device name listed in this FDA 510(k) record. The listed applicant is Citicare Systems, Inc.. It received FDA 510(k) clearance on 1993-03-10 under 510(k) number K924083. 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 700/700-1?

700/700-1 is a medical device that received FDA 510(k) clearance on 1993-03-10. The listed applicant is Citicare Systems, Inc.. The 510(k) number is K924083.

When did 700/700-1 receive FDA 510(k) clearance?

700/700-1 received FDA 510(k) clearance on 1993-03-10, under 510(k) number K924083.

Who is the listed applicant for 700/700-1?

The FDA 510(k) record lists Citicare Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 700/700-1?

The FDA product code for 700/700-1 is CCK.

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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