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PROSTHOFLEX

Page Type
Cleared 510(K)
510(k) Number
K942562
510(k) Type
Traditional
Applicant
KNOPF ASSOC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/20/1994
Days to Decision
203 days
Submission Type
Statement

PROSTHOFLEX

Page Type
Cleared 510(K)
510(k) Number
K942562
510(k) Type
Traditional
Applicant
KNOPF ASSOC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/20/1994
Days to Decision
203 days
Submission Type
Statement