UMBRELLA WALKER
K-Number: K833195 · 1983-10-27
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Device Summary
Frequently Asked Questions
What is the UMBRELLA WALKER?
UMBRELLA WALKER is a medical device that received FDA 510(k) clearance on 1983-10-27. The listed applicant is Convaid Products, Inc.. The 510(k) number is K833195.
When did UMBRELLA WALKER receive FDA 510(k) clearance?
UMBRELLA WALKER received FDA 510(k) clearance on 1983-10-27, under 510(k) number K833195.
Who is the listed applicant for UMBRELLA WALKER?
The FDA 510(k) record lists Convaid Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for UMBRELLA WALKER?
The FDA product code for UMBRELLA 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 Convaid Products, 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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