SHERPA/KODIAK CUB MOBILITY SYSTEM (MANUAL WHEELCHAIR)
K-Number: K001890 · 2000-07-24
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Device Summary
Frequently Asked Questions
What is the SHERPA/KODIAK CUB MOBILITY SYSTEM (MANUAL WHEELCHAIR)?
SHERPA/KODIAK CUB MOBILITY SYSTEM (MANUAL WHEELCHAIR) is a medical device that received FDA 510(k) clearance on 2000-07-24. The listed applicant is Otto Bock Orthopaedische Industrie, Kg.. The 510(k) number is K001890.
When did SHERPA/KODIAK CUB MOBILITY SYSTEM (MANUAL WHEELCHAIR) receive FDA 510(k) clearance?
SHERPA/KODIAK CUB MOBILITY SYSTEM (MANUAL WHEELCHAIR) received FDA 510(k) clearance on 2000-07-24, under 510(k) number K001890.
Who is the listed applicant for SHERPA/KODIAK CUB MOBILITY SYSTEM (MANUAL WHEELCHAIR)?
The FDA 510(k) record lists Otto Bock Orthopaedische Industrie, Kg. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SHERPA/KODIAK CUB MOBILITY SYSTEM (MANUAL WHEELCHAIR)?
The FDA product code for SHERPA/KODIAK CUB MOBILITY SYSTEM (MANUAL 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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