SRX COMP ULTRALIGHT WHEELCHAIR
K-Number: K932927 · 1993-07-22
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Device Summary
Frequently Asked Questions
What is the SRX COMP ULTRALIGHT WHEELCHAIR?
SRX COMP ULTRALIGHT WHEELCHAIR is a medical device that received FDA 510(k) clearance on 1993-07-22. The listed applicant is Medical Composite Technology, Inc.. The 510(k) number is K932927.
When did SRX COMP ULTRALIGHT WHEELCHAIR receive FDA 510(k) clearance?
SRX COMP ULTRALIGHT WHEELCHAIR received FDA 510(k) clearance on 1993-07-22, under 510(k) number K932927.
Who is the listed applicant for SRX COMP ULTRALIGHT WHEELCHAIR?
The FDA 510(k) record lists Medical Composite Technology, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SRX COMP ULTRALIGHT WHEELCHAIR?
The FDA product code for SRX COMP ULTRALIGHT 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.
Other records listing Medical Composite Technology, 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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