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SPECIMEN REMOVAL DEVICE

Page Type
Cleared 510(K)
510(k) Number
K941249
510(k) Type
Traditional
Applicant
GENERAL SURGICAL INNOVATIONS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/7/1994
Days to Decision
114 days
Submission Type
Summary

SPECIMEN REMOVAL DEVICE

Page Type
Cleared 510(K)
510(k) Number
K941249
510(k) Type
Traditional
Applicant
GENERAL SURGICAL INNOVATIONS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/7/1994
Days to Decision
114 days
Submission Type
Summary