Last synced on 14 November 2025 at 11:06 pm

KODNER ANAL PERIONEAL RETRACTOR

Page Type
Cleared 510(K)
510(k) Number
K870897
510(k) Type
Traditional
Applicant
SUR-MED INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/4/1987
Days to Decision
91 days

KODNER ANAL PERIONEAL RETRACTOR

Page Type
Cleared 510(K)
510(k) Number
K870897
510(k) Type
Traditional
Applicant
SUR-MED INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/4/1987
Days to Decision
91 days