WALL TRANSFORMERS 74710 & 74910
K-Number: K771864 · 1977-11-22
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Device Summary
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.
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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