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FDA 510(k)

GAS-LYTE 1CC AND 3CC ARTERIAL BLOOD SAMPLERS

K-Number: K902632 · 1990-09-04

ApplicantMarquest Medical Products, Inc.
Decision Date1990-09-04
Product CodeCBT
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

GAS-LYTE 1CC AND 3CC ARTERIAL BLOOD SAMPLERS is the device name listed in this FDA 510(k) record. The listed applicant is Marquest Medical Products, Inc.. It received FDA 510(k) clearance on 1990-09-04 under 510(k) number K902632. The device is classified under product code CBT. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GAS-LYTE 1CC AND 3CC ARTERIAL BLOOD SAMPLERS?

GAS-LYTE 1CC AND 3CC ARTERIAL BLOOD SAMPLERS is a medical device that received FDA 510(k) clearance on 1990-09-04. The listed applicant is Marquest Medical Products, Inc.. The 510(k) number is K902632.

When did GAS-LYTE 1CC AND 3CC ARTERIAL BLOOD SAMPLERS receive FDA 510(k) clearance?

GAS-LYTE 1CC AND 3CC ARTERIAL BLOOD SAMPLERS received FDA 510(k) clearance on 1990-09-04, under 510(k) number K902632.

Who is the listed applicant for GAS-LYTE 1CC AND 3CC ARTERIAL BLOOD SAMPLERS?

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

What is the FDA product code for GAS-LYTE 1CC AND 3CC ARTERIAL BLOOD SAMPLERS?

The FDA product code for GAS-LYTE 1CC AND 3CC ARTERIAL BLOOD SAMPLERS is CBT.

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Other records listing Marquest Medical Products, 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.

K050066C-CO2 COLORIMETRIC CO2 INDICATORK970478SCT 3000 HEATED HUMIDIFIERK962220HEATED WIRE CIRCUITS FOR SCT 3000 HEATED HUMIDIFIERK962223WATER CHAMBERS FOR ST 3000 HEATED HUMIDIFIERK960972DISPOSABLE GAS SAMPLING INTERFACE KITSK961838RESPIRGARD II, SPIROGARD

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Related Devices (Code: CBT)

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.

K071269HEMODRAW ARTERIAL BLOOD SAMPLING SYSTEMSmiths Medical Asd, Inc.K070340SECURE ARTERIAL BLOOD SAMPLING SYSTEMSmiths Medical Asd, Inc.K955663ABC IN-LINE BLOOD SAMPLING KITUtah Medical Products, Inc.K954015ABG POINT LOK NEEDLE PROTECTION DEVICEDevon Industries, Inc.K954035ACTI-FLEX ARTERIAL EXTENSION SETR-Group Intl.K950098NEEDLE SAFETY COVERHammer-Plane, 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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