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FDA 510(k)

ARTAP ARTERIAL BLOOD SAMPLING DEVICE

K-Number: K843360 · 1984-10-31

ApplicantAnalytical Products, Inc.
Decision Date1984-10-31
Product CodeCBT
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ARTAP ARTERIAL BLOOD SAMPLING DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Analytical Products, Inc.. It received FDA 510(k) clearance on 1984-10-31 under 510(k) number K843360. 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 ARTAP ARTERIAL BLOOD SAMPLING DEVICE?

ARTAP ARTERIAL BLOOD SAMPLING DEVICE is a medical device that received FDA 510(k) clearance on 1984-10-31. The listed applicant is Analytical Products, Inc.. The 510(k) number is K843360.

When did ARTAP ARTERIAL BLOOD SAMPLING DEVICE receive FDA 510(k) clearance?

ARTAP ARTERIAL BLOOD SAMPLING DEVICE received FDA 510(k) clearance on 1984-10-31, under 510(k) number K843360.

Who is the listed applicant for ARTAP ARTERIAL BLOOD SAMPLING DEVICE?

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

What is the FDA product code for ARTAP ARTERIAL BLOOD SAMPLING DEVICE?

The FDA product code for ARTAP ARTERIAL BLOOD SAMPLING DEVICE is CBT.

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Other records listing Analytical Products, Inc. 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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