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HI-RIDER WHEELCHAIR

Page Type
Cleared 510(K)
510(k) Number
K890695
510(k) Type
Traditional
Applicant
RETEC USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/10/1989
Days to Decision
59 days

HI-RIDER WHEELCHAIR

Page Type
Cleared 510(K)
510(k) Number
K890695
510(k) Type
Traditional
Applicant
RETEC USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/10/1989
Days to Decision
59 days