SHOCKWAVE SUSPENSION WHEELCHAIR
K-Number: K032123 · 2003-07-31
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Device Summary
Frequently Asked Questions
What is the SHOCKWAVE SUSPENSION WHEELCHAIR?
SHOCKWAVE SUSPENSION WHEELCHAIR is a medical device that received FDA 510(k) clearance on 2003-07-31. The listed applicant is Per4max Medical, LLC. The 510(k) number is K032123.
When did SHOCKWAVE SUSPENSION WHEELCHAIR receive FDA 510(k) clearance?
SHOCKWAVE SUSPENSION WHEELCHAIR received FDA 510(k) clearance on 2003-07-31, under 510(k) number K032123.
Who is the listed applicant for SHOCKWAVE SUSPENSION WHEELCHAIR?
The FDA 510(k) record lists Per4max Medical, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SHOCKWAVE SUSPENSION WHEELCHAIR?
The FDA product code for SHOCKWAVE SUSPENSION WHEELCHAIR 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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