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KENLOR HUMAN SPINAL FLUID CONTROL LIQUID

Page Type
Cleared 510(K)
510(k) Number
K890576
510(k) Type
Traditional
Applicant
KENLOR INDUSTRIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/9/1989
Days to Decision
31 days

KENLOR HUMAN SPINAL FLUID CONTROL LIQUID

Page Type
Cleared 510(K)
510(k) Number
K890576
510(k) Type
Traditional
Applicant
KENLOR INDUSTRIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/9/1989
Days to Decision
31 days