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PETERS CARDIONYL(TM) SUTURE

Page Type
Cleared 510(K)
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)
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