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STORZ DAISYPLUS SERIES MICROSURGICAL SYSTEMS

Page Type
Cleared 510(K)
510(k) Number
K894278
510(k) Type
Traditional
Applicant
STORZ INSTRUMENT CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/11/1989
Days to Decision
49 days

STORZ DAISYPLUS SERIES MICROSURGICAL SYSTEMS

Page Type
Cleared 510(K)
510(k) Number
K894278
510(k) Type
Traditional
Applicant
STORZ INSTRUMENT CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/11/1989
Days to Decision
49 days