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MODIFIED AIR FLUIDIZED BED, KINAIR

Page Type
Cleared 510(K)
510(k) Number
K880340
510(k) Type
Traditional
Applicant
KINETIC CONCEPTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/16/1988
Days to Decision
21 days

MODIFIED AIR FLUIDIZED BED, KINAIR

Page Type
Cleared 510(K)
510(k) Number
K880340
510(k) Type
Traditional
Applicant
KINETIC CONCEPTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/16/1988
Days to Decision
21 days