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FDA 510(k)

DESERET ARTERIAL BLOOD SAMPLING KIT

K-Number: K822248 · 1982-10-21

ApplicantWarner-Lambert Co.
Decision Date1982-10-21
Product CodeCBT
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

DESERET ARTERIAL BLOOD SAMPLING KIT is the device name listed in this FDA 510(k) record. The listed applicant is Warner-Lambert Co.. It received FDA 510(k) clearance on 1982-10-21 under 510(k) number K822248. 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 DESERET ARTERIAL BLOOD SAMPLING KIT?

DESERET ARTERIAL BLOOD SAMPLING KIT is a medical device that received FDA 510(k) clearance on 1982-10-21. The listed applicant is Warner-Lambert Co.. The 510(k) number is K822248.

When did DESERET ARTERIAL BLOOD SAMPLING KIT receive FDA 510(k) clearance?

DESERET ARTERIAL BLOOD SAMPLING KIT received FDA 510(k) clearance on 1982-10-21, under 510(k) number K822248.

Who is the listed applicant for DESERET ARTERIAL BLOOD SAMPLING KIT?

The FDA 510(k) record lists Warner-Lambert Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DESERET ARTERIAL BLOOD SAMPLING KIT?

The FDA product code for DESERET ARTERIAL BLOOD SAMPLING KIT is CBT.

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Other records listing Warner-Lambert Co. as applicant

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K024160NEOSPORIN SCAR SOLUTIONK893452EXTRA STRENGTH EFFERGRIP DENTURE ADHESIVE CREAMK870584O.P.T.(TM) OVULATION PREDICTION TESTK861510MULTILUMEN VIAPIC CENTRAL LINE CATHETERK852689GENERAL DIAGNOSTICS CEFTAZIDIME 30 MCG SUSC DISKK852967GENERAL DIAGNOSTICS' CEFTRIAXONE 30MCG SUSDEP DISK

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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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