WH CONVERTIBLE LIGHTWEGHT WHEELCHAIR, MODEL WHL100
K-Number: K060251 · 2006-03-08
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Device Summary
Frequently Asked Questions
What is the WH CONVERTIBLE LIGHTWEGHT WHEELCHAIR, MODEL WHL100?
WH CONVERTIBLE LIGHTWEGHT WHEELCHAIR, MODEL WHL100 is a medical device that received FDA 510(k) clearance on 2006-03-08. The listed applicant is Well Home Health Products Co.. The 510(k) number is K060251.
When did WH CONVERTIBLE LIGHTWEGHT WHEELCHAIR, MODEL WHL100 receive FDA 510(k) clearance?
WH CONVERTIBLE LIGHTWEGHT WHEELCHAIR, MODEL WHL100 received FDA 510(k) clearance on 2006-03-08, under 510(k) number K060251.
Who is the listed applicant for WH CONVERTIBLE LIGHTWEGHT WHEELCHAIR, MODEL WHL100?
The FDA 510(k) record lists Well Home Health Products Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for WH CONVERTIBLE LIGHTWEGHT WHEELCHAIR, MODEL WHL100?
The FDA product code for WH CONVERTIBLE LIGHTWEGHT WHEELCHAIR, MODEL WHL100 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.
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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