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FDA 510(k)

QS90 SMOOTH E ARTERIAL BLOOD SAMPLER

K-Number: K896514 · 1990-01-23

ApplicantRadiometer America, Inc.
Decision Date1990-01-23
Product CodeGIM
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

QS90 SMOOTH E ARTERIAL BLOOD SAMPLER is the device name listed in this FDA 510(k) record. The listed applicant is Radiometer America, Inc.. It received FDA 510(k) clearance on 1990-01-23 under 510(k) number K896514. The device is classified under product code GIM. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QS90 SMOOTH E ARTERIAL BLOOD SAMPLER?

QS90 SMOOTH E ARTERIAL BLOOD SAMPLER is a medical device that received FDA 510(k) clearance on 1990-01-23. The listed applicant is Radiometer America, Inc.. The 510(k) number is K896514.

When did QS90 SMOOTH E ARTERIAL BLOOD SAMPLER receive FDA 510(k) clearance?

QS90 SMOOTH E ARTERIAL BLOOD SAMPLER received FDA 510(k) clearance on 1990-01-23, under 510(k) number K896514.

Who is the listed applicant for QS90 SMOOTH E ARTERIAL BLOOD SAMPLER?

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

What is the FDA product code for QS90 SMOOTH E ARTERIAL BLOOD SAMPLER?

The FDA product code for QS90 SMOOTH E ARTERIAL BLOOD SAMPLER is GIM.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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