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GE MEDICAL-NEEDLE GUIDE FOR SV, TR ANDATF, ACUSON-NEEDLE GUIDE

Page Type
Cleared 510(K)
510(k) Number
K971115
510(k) Type
Traditional
Applicant
PROTEK MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/13/1997
Days to Decision
78 days
Submission Type
Summary

GE MEDICAL-NEEDLE GUIDE FOR SV, TR ANDATF, ACUSON-NEEDLE GUIDE

Page Type
Cleared 510(K)
510(k) Number
K971115
510(k) Type
Traditional
Applicant
PROTEK MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/13/1997
Days to Decision
78 days
Submission Type
Summary