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STAGE ZERO AIR FLOTATION BED

Page Type
Cleared 510(K)
510(k) Number
K905053
510(k) Type
Traditional
Applicant
LAKE MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/26/1990
Days to Decision
18 days

STAGE ZERO AIR FLOTATION BED

Page Type
Cleared 510(K)
510(k) Number
K905053
510(k) Type
Traditional
Applicant
LAKE MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/26/1990
Days to Decision
18 days