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FDA 510(k), K171334, Indego
FDA 510(k), K171334, Indego
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510(K) Number: K171334
Device Name: Indego
Manufacturer: Parker Hannifin Corporation
Device Classification Name: powered exoskeleton
Regulation Number: 890.3480
Classification Product Code: PHL
Date Received: 05/08/2017
Decision Date: 09/08/2017
Regulation Medical Specialty: Physical Medicine
Device Name: Indego
Manufacturer: Parker Hannifin Corporation
Device Classification Name: powered exoskeleton
Regulation Number: 890.3480
Classification Product Code: PHL
Date Received: 05/08/2017
Decision Date: 09/08/2017
Regulation Medical Specialty: Physical Medicine
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- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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