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KENLOR HUMAN SPINAL FLUID CONTROL LIQUID

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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