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ANTIMICROBIAL REMOVAL DEVICE

Page Type
Cleared 510(K)
510(k) Number
K810613
510(k) Type
Traditional
Applicant
MARION LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/3/1981
Days to Decision
28 days

ANTIMICROBIAL REMOVAL DEVICE

Page Type
Cleared 510(K)
510(k) Number
K810613
510(k) Type
Traditional
Applicant
MARION LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/3/1981
Days to Decision
28 days