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SYSTEM 3000 FLUIDIZED AIR BED

Page Type
Cleared 510(K)
510(k) Number
K890935
510(k) Type
Traditional
Applicant
DERMANETICS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/15/1989
Days to Decision
19 days

SYSTEM 3000 FLUIDIZED AIR BED

Page Type
Cleared 510(K)
510(k) Number
K890935
510(k) Type
Traditional
Applicant
DERMANETICS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/15/1989
Days to Decision
19 days