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KENLOR HUMAN SPINAL FLUID CONTROL

Page Type
Cleared 510(K)
510(k) Number
K950326
510(k) Type
Traditional
Applicant
KENLOR INDUSTRIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/20/1995
Days to Decision
61 days
Submission Type
Statement

KENLOR HUMAN SPINAL FLUID CONTROL

Page Type
Cleared 510(K)
510(k) Number
K950326
510(k) Type
Traditional
Applicant
KENLOR INDUSTRIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/20/1995
Days to Decision
61 days
Submission Type
Statement