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FIBERFILL AGP

Page Type
Cleared 510(K)
510(k) Number
K023818
510(k) Type
Traditional
Applicant
PENTRON CLINICAL TECHNOLOGIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/3/2003
Days to Decision
139 days
Submission Type
Statement

FIBERFILL AGP

Page Type
Cleared 510(K)
510(k) Number
K023818
510(k) Type
Traditional
Applicant
PENTRON CLINICAL TECHNOLOGIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/3/2003
Days to Decision
139 days
Submission Type
Statement