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ARGUS LAPAROSCOPY INSTRUMENT SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K950378
510(k) Type
Traditional
Applicant
ARGUS MEDICAL CO., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/9/1995
Days to Decision
9 days
Submission Type
Statement

ARGUS LAPAROSCOPY INSTRUMENT SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K950378
510(k) Type
Traditional
Applicant
ARGUS MEDICAL CO., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/9/1995
Days to Decision
9 days
Submission Type
Statement