LIGHT WEIGHT ALUMINUM WALKER
K-Number: K821404 · 1982-05-21
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Device Summary
Frequently Asked Questions
What is the LIGHT WEIGHT ALUMINUM WALKER?
LIGHT WEIGHT ALUMINUM WALKER is a medical device that received FDA 510(k) clearance on 1982-05-21. The listed applicant is Manuco Manufacturing Co., Inc.. The 510(k) number is K821404.
When did LIGHT WEIGHT ALUMINUM WALKER receive FDA 510(k) clearance?
LIGHT WEIGHT ALUMINUM WALKER received FDA 510(k) clearance on 1982-05-21, under 510(k) number K821404.
Who is the listed applicant for LIGHT WEIGHT ALUMINUM WALKER?
The FDA 510(k) record lists Manuco Manufacturing Co., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LIGHT WEIGHT ALUMINUM WALKER?
The FDA product code for LIGHT WEIGHT ALUMINUM WALKER is ITJ.
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 Manuco Manufacturing Co., 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.
Related Devices (Code: ITJ)
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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