UROK ROCKING WHEELCHAIR, MODEL 700-4XX
K-Number: K052548 · 2006-01-06
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Device Summary
Frequently Asked Questions
What is the UROK ROCKING WHEELCHAIR, MODEL 700-4XX?
UROK ROCKING WHEELCHAIR, MODEL 700-4XX is a medical device that received FDA 510(k) clearance on 2006-01-06. The listed applicant is Amg Medical, Inc.. The 510(k) number is K052548.
When did UROK ROCKING WHEELCHAIR, MODEL 700-4XX receive FDA 510(k) clearance?
UROK ROCKING WHEELCHAIR, MODEL 700-4XX received FDA 510(k) clearance on 2006-01-06, under 510(k) number K052548.
Who is the listed applicant for UROK ROCKING WHEELCHAIR, MODEL 700-4XX?
The FDA 510(k) record lists Amg Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for UROK ROCKING WHEELCHAIR, MODEL 700-4XX?
The FDA product code for UROK ROCKING WHEELCHAIR, MODEL 700-4XX is IOR.
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 Amg Medical, 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: IOR)
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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