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FDA 510(k)

MICROPAQ, MODELS 402, 404

K-Number: K021681 · 2002-07-23

Decision Date2002-07-23
Product CodeDRT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MICROPAQ, MODELS 402, 404 is the device name listed in this FDA 510(k) record. The listed applicant is Welch Allyn Protocol, Inc.. It received FDA 510(k) clearance on 2002-07-23 under 510(k) number K021681. The device is classified under product code DRT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICROPAQ, MODELS 402, 404?

MICROPAQ, MODELS 402, 404 is a medical device that received FDA 510(k) clearance on 2002-07-23. The listed applicant is Welch Allyn Protocol, Inc.. The 510(k) number is K021681.

When did MICROPAQ, MODELS 402, 404 receive FDA 510(k) clearance?

MICROPAQ, MODELS 402, 404 received FDA 510(k) clearance on 2002-07-23, under 510(k) number K021681.

Who is the listed applicant for MICROPAQ, MODELS 402, 404?

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

What is the FDA product code for MICROPAQ, MODELS 402, 404?

The FDA product code for MICROPAQ, MODELS 402, 404 is DRT.

Related Clinical Trials

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.

Other records listing Welch Allyn Protocol, Inc. as applicant

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.

View all 7 devices →

Related Devices (Code: DRT)

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.

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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