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PROGUIDE NEEDLE SET

Page Type
Cleared 510(K)
510(k) Number
K060349
510(k) Type
Special
Applicant
NUCLETRON CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/10/2006
Days to Decision
28 days
Submission Type
Summary

PROGUIDE NEEDLE SET

Page Type
Cleared 510(K)
510(k) Number
K060349
510(k) Type
Special
Applicant
NUCLETRON CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/10/2006
Days to Decision
28 days
Submission Type
Summary