Last synced on 25 January 2026 at 3:41 am

FIBREKOR

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K964578
510(k) Type
Traditional
Applicant
Jeneric/Pentron, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/3/1996
Days to Decision
18 days
Submission Type
Statement

FIBREKOR

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K964578
510(k) Type
Traditional
Applicant
Jeneric/Pentron, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/3/1996
Days to Decision
18 days
Submission Type
Statement