ROLLS 3000 SERIES WHEELCHAIR (YOUTHMOBILE)
K-Number: K884931 · 1988-12-12
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Device Summary
Frequently Asked Questions
What is the ROLLS 3000 SERIES WHEELCHAIR (YOUTHMOBILE)?
ROLLS 3000 SERIES WHEELCHAIR (YOUTHMOBILE) is a medical device that received FDA 510(k) clearance on 1988-12-12. The listed applicant is Invacare Corp.. The 510(k) number is K884931.
When did ROLLS 3000 SERIES WHEELCHAIR (YOUTHMOBILE) receive FDA 510(k) clearance?
ROLLS 3000 SERIES WHEELCHAIR (YOUTHMOBILE) received FDA 510(k) clearance on 1988-12-12, under 510(k) number K884931.
Who is the listed applicant for ROLLS 3000 SERIES WHEELCHAIR (YOUTHMOBILE)?
The FDA 510(k) record lists Invacare Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ROLLS 3000 SERIES WHEELCHAIR (YOUTHMOBILE)?
The FDA product code for ROLLS 3000 SERIES WHEELCHAIR (YOUTHMOBILE) 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 Invacare Corp. 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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