STANDARD WHEELCHAIR
K-Number: K963301 · 1996-10-23
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Device Summary
Frequently Asked Questions
What is the STANDARD WHEELCHAIR?
STANDARD WHEELCHAIR is a medical device that received FDA 510(k) clearance on 1996-10-23. The listed applicant is L & M Resource Information Service, Inc.. The 510(k) number is K963301.
When did STANDARD WHEELCHAIR receive FDA 510(k) clearance?
STANDARD WHEELCHAIR received FDA 510(k) clearance on 1996-10-23, under 510(k) number K963301.
Who is the listed applicant for STANDARD WHEELCHAIR?
The FDA 510(k) record lists L & M Resource Information Service, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for STANDARD WHEELCHAIR?
The FDA product code for STANDARD 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 L & M Resource Information Service, 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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