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MEDIFIX SINGLE AND DOUBLE PUNCTURE LAPAROSCOPES

Page Type
Cleared 510(K)
510(k) Number
K992480
510(k) Type
Traditional
Applicant
MEDIFIX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/23/1999
Days to Decision
59 days
Submission Type
Statement

MEDIFIX SINGLE AND DOUBLE PUNCTURE LAPAROSCOPES

Page Type
Cleared 510(K)
510(k) Number
K992480
510(k) Type
Traditional
Applicant
MEDIFIX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/23/1999
Days to Decision
59 days
Submission Type
Statement