FDA 510(k), K971873, LEVO ACTIVE-EASY LAE

FDA 510(k), K971873, LEVO ACTIVE-EASY LAE

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510(K) Number: K971873
Device Name: LEVO ACTIVE-EASY LAE
Manufacturer:
Device Classification Name: Wheelchair, Standup
Regulation Number: 890.3900
Classification Product Code: IPL
Date Received: 05/20/1997
Decision Date: 07/03/1997
Regulation Medical Specialty: Physical Medicine
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