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STORZ PREMIERE II MICROSURGICAL SYSTEM (CX SERIES)

Page Type
Cleared 510(K)
510(k) Number
K961310
510(k) Type
Traditional
Applicant
STORZ INSTRUMENT CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/27/1996
Days to Decision
84 days
Submission Type
Summary

STORZ PREMIERE II MICROSURGICAL SYSTEM (CX SERIES)

Page Type
Cleared 510(K)
510(k) Number
K961310
510(k) Type
Traditional
Applicant
STORZ INSTRUMENT CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/27/1996
Days to Decision
84 days
Submission Type
Summary