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LAPAROSCOPY DILATION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K942201
510(k) Type
Traditional
Applicant
RICHARD WOLF MEDICAL INSTRUMENTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/25/1994
Days to Decision
20 days
Submission Type
Statement

LAPAROSCOPY DILATION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K942201
510(k) Type
Traditional
Applicant
RICHARD WOLF MEDICAL INSTRUMENTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/25/1994
Days to Decision
20 days
Submission Type
Statement