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INSTRUMENT, MANUAL, GENERAL SURGICAL

Page Type
Cleared 510(K)
510(k) Number
K925707
510(k) Type
Traditional
Applicant
SYMBIOSIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/26/1993
Days to Decision
195 days
Submission Type
Statement

INSTRUMENT, MANUAL, GENERAL SURGICAL

Page Type
Cleared 510(K)
510(k) Number
K925707
510(k) Type
Traditional
Applicant
SYMBIOSIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/26/1993
Days to Decision
195 days
Submission Type
Statement