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PETERS CARDIONYL(TM) SUTURE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K913102
510(k) Type
Traditional
Applicant
PROMEDICA PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/3/1992
Days to Decision
388 days
Submission Type
Statement

PETERS CARDIONYL(TM) SUTURE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K913102
510(k) Type
Traditional
Applicant
PROMEDICA PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/3/1992
Days to Decision
388 days
Submission Type
Statement