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RE-NEW LAPAROSCOPIC INSTRUMENTS

Page Type
Cleared 510(K)
510(k) Number
K962119
510(k) Type
Traditional
Applicant
MICROLINE PENTAX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/9/1996
Days to Decision
70 days
Submission Type
Summary

RE-NEW LAPAROSCOPIC INSTRUMENTS

Page Type
Cleared 510(K)
510(k) Number
K962119
510(k) Type
Traditional
Applicant
MICROLINE PENTAX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/9/1996
Days to Decision
70 days
Submission Type
Summary