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FDA 510(k)

LINK TO ACUITY CLINICIAN NOTIFIER

K-Number: K070204 · 2007-03-23

ApplicantWelch Allyn Protocol, Inc.
Decision Date2007-03-23
Product CodeMSX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

LINK TO ACUITY CLINICIAN NOTIFIER 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 2007-03-23 under 510(k) number K070204. The device is classified under product code MSX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LINK TO ACUITY CLINICIAN NOTIFIER?

LINK TO ACUITY CLINICIAN NOTIFIER is a medical device that received FDA 510(k) clearance on 2007-03-23. The listed applicant is Welch Allyn Protocol, Inc.. The 510(k) number is K070204.

When did LINK TO ACUITY CLINICIAN NOTIFIER receive FDA 510(k) clearance?

LINK TO ACUITY CLINICIAN NOTIFIER received FDA 510(k) clearance on 2007-03-23, under 510(k) number K070204.

Who is the listed applicant for LINK TO ACUITY CLINICIAN NOTIFIER?

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 LINK TO ACUITY CLINICIAN NOTIFIER?

The FDA product code for LINK TO ACUITY CLINICIAN NOTIFIER is MSX.

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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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