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FDA 510(k)

ATLAS MONITOR, MODELS 200,210,220

K-Number: K022084 · 2002-09-26

ApplicantWelch Allyn, Inc.
Decision Date2002-09-26
Product CodeDQA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ATLAS MONITOR, MODELS 200,210,220 is the device name listed in this FDA 510(k) record. The listed applicant is Welch Allyn, Inc.. It received FDA 510(k) clearance on 2002-09-26 under 510(k) number K022084. The device is classified under product code DQA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ATLAS MONITOR, MODELS 200,210,220?

ATLAS MONITOR, MODELS 200,210,220 is a medical device that received FDA 510(k) clearance on 2002-09-26. The listed applicant is Welch Allyn, Inc.. The 510(k) number is K022084.

When did ATLAS MONITOR, MODELS 200,210,220 receive FDA 510(k) clearance?

ATLAS MONITOR, MODELS 200,210,220 received FDA 510(k) clearance on 2002-09-26, under 510(k) number K022084.

Who is the listed applicant for ATLAS MONITOR, MODELS 200,210,220?

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

What is the FDA product code for ATLAS MONITOR, MODELS 200,210,220?

The FDA product code for ATLAS MONITOR, MODELS 200,210,220 is DQA.

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Other records listing Welch Allyn, Inc. as applicant

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Related Devices (Code: DQA)

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.

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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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