Last synced on 20 December 2024 at 11:05 pm

SPECIMEN REMOVAL DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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