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MODIFIED PRISTINE CULTURE CATHETER

Page Type
Cleared 510(K)
510(k) Number
K893390
510(k) Type
Traditional
Applicant
HML MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/7/1989
Days to Decision
129 days

MODIFIED PRISTINE CULTURE CATHETER

Page Type
Cleared 510(K)
510(k) Number
K893390
510(k) Type
Traditional
Applicant
HML MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/7/1989
Days to Decision
129 days