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FDA 510(k)

DRI-VENDT/PROVENT/ACCUVENT ARTERIAL BLOOD GAS KITS

K-Number: K930286 · 1993-06-22

ApplicantConcord/Portex
Decision Date1993-06-22
Product CodeCBT
Advisory CommitteeAN
DecisionUnknown

Device Summary

DRI-VENDT/PROVENT/ACCUVENT ARTERIAL BLOOD GAS KITS is the device name listed in this FDA 510(k) record. The listed applicant is Concord/Portex. It received FDA 510(k) clearance on 1993-06-22 under 510(k) number K930286. The device is classified under product code CBT. It was reviewed by the AN advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the DRI-VENDT/PROVENT/ACCUVENT ARTERIAL BLOOD GAS KITS?

DRI-VENDT/PROVENT/ACCUVENT ARTERIAL BLOOD GAS KITS is a medical device that received FDA 510(k) clearance on 1993-06-22. The listed applicant is Concord/Portex. The 510(k) number is K930286.

When did DRI-VENDT/PROVENT/ACCUVENT ARTERIAL BLOOD GAS KITS receive FDA 510(k) clearance?

DRI-VENDT/PROVENT/ACCUVENT ARTERIAL BLOOD GAS KITS received FDA 510(k) clearance on 1993-06-22, under 510(k) number K930286.

Who is the listed applicant for DRI-VENDT/PROVENT/ACCUVENT ARTERIAL BLOOD GAS KITS?

The FDA 510(k) record lists Concord/Portex as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DRI-VENDT/PROVENT/ACCUVENT ARTERIAL BLOOD GAS KITS?

The FDA product code for DRI-VENDT/PROVENT/ACCUVENT ARTERIAL BLOOD GAS KITS is CBT.

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Other records listing Concord/Portex as applicant

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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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