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FDA 510(k)

WELCH ALLYN CARDIOPERFECT WORKSTATION SOFTWARE (CPWS) V 1.62

K-Number: K082478 · 2009-03-09

Decision Date2009-03-09
Product CodeBZG
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

WELCH ALLYN CARDIOPERFECT WORKSTATION SOFTWARE (CPWS) V 1.62 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 2009-03-09 under 510(k) number K082478. The device is classified under product code BZG. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WELCH ALLYN CARDIOPERFECT WORKSTATION SOFTWARE (CPWS) V 1.62?

WELCH ALLYN CARDIOPERFECT WORKSTATION SOFTWARE (CPWS) V 1.62 is a medical device that received FDA 510(k) clearance on 2009-03-09. The listed applicant is Welch Allyn, Inc.. The 510(k) number is K082478.

When did WELCH ALLYN CARDIOPERFECT WORKSTATION SOFTWARE (CPWS) V 1.62 receive FDA 510(k) clearance?

WELCH ALLYN CARDIOPERFECT WORKSTATION SOFTWARE (CPWS) V 1.62 received FDA 510(k) clearance on 2009-03-09, under 510(k) number K082478.

Who is the listed applicant for WELCH ALLYN CARDIOPERFECT WORKSTATION SOFTWARE (CPWS) V 1.62?

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 WELCH ALLYN CARDIOPERFECT WORKSTATION SOFTWARE (CPWS) V 1.62?

The FDA product code for WELCH ALLYN CARDIOPERFECT WORKSTATION SOFTWARE (CPWS) V 1.62 is BZG.

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, 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.

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Related Devices (Code: BZG)

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

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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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