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FDA 510(k)

ENGSTROM ELIZA + CO2 ANALYZER

K-Number: K890112 · 1989-03-15

ApplicantGambro, Inc.
Decision Date1989-03-15
Product CodeCCK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ENGSTROM ELIZA + CO2 ANALYZER is the device name listed in this FDA 510(k) record. The listed applicant is Gambro, Inc.. It received FDA 510(k) clearance on 1989-03-15 under 510(k) number K890112. 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 ENGSTROM ELIZA + CO2 ANALYZER?

ENGSTROM ELIZA + CO2 ANALYZER is a medical device that received FDA 510(k) clearance on 1989-03-15. The listed applicant is Gambro, Inc.. The 510(k) number is K890112.

When did ENGSTROM ELIZA + CO2 ANALYZER receive FDA 510(k) clearance?

ENGSTROM ELIZA + CO2 ANALYZER received FDA 510(k) clearance on 1989-03-15, under 510(k) number K890112.

Who is the listed applicant for ENGSTROM ELIZA + CO2 ANALYZER?

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

What is the FDA product code for ENGSTROM ELIZA + CO2 ANALYZER?

The FDA product code for ENGSTROM ELIZA + CO2 ANALYZER is CCK.

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Other records listing Gambro, 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.

K083158EXALIS, SOFTWARE VERSION 1.15K070643PHOENIX HEMODIALYSIS DELIVERY SYSTEM, VERSION 3.35K032431PRISMA M60/M100 SETSK896758GAMBRO BICARBONATE MONITOR BCM 10-3K896757GAMBRO AK-10 DIALYSIS SYSTEM FOR HIGH FLOWSK902481GAMBRO ALWALL GFS PLUS 11, 16 & 20 HOLLOW FIBER

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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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