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FDA 510(k)

WALL TRANSFORMERS 74710 & 74910

K-Number: K771864 · 1977-11-22

Decision Date1977-11-22
Product CodeGCW
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

WALL TRANSFORMERS 74710 & 74910 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 1977-11-22 under 510(k) number K771864. The device is classified under product code GCW. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WALL TRANSFORMERS 74710 & 74910?

WALL TRANSFORMERS 74710 & 74910 is a medical device that received FDA 510(k) clearance on 1977-11-22. The listed applicant is Welch Allyn, Inc.. The 510(k) number is K771864.

When did WALL TRANSFORMERS 74710 & 74910 receive FDA 510(k) clearance?

WALL TRANSFORMERS 74710 & 74910 received FDA 510(k) clearance on 1977-11-22, under 510(k) number K771864.

Who is the listed applicant for WALL TRANSFORMERS 74710 & 74910?

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 WALL TRANSFORMERS 74710 & 74910?

The FDA product code for WALL TRANSFORMERS 74710 & 74910 is GCW.

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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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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