Last synced on 14 November 2025 at 11:06 pm

PETERS CARDIOFLON(TM) SUTURE

Page Type
Cleared 510(K)
510(k) Number
K913101
510(k) Type
Traditional
Applicant
PROMEDICA PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/12/1992
Days to Decision
397 days
Submission Type
Statement

PETERS CARDIOFLON(TM) SUTURE

Page Type
Cleared 510(K)
510(k) Number
K913101
510(k) Type
Traditional
Applicant
PROMEDICA PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/12/1992
Days to Decision
397 days
Submission Type
Statement