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ULTRAGUIDE 1000

Page Type
Cleared 510(K)
510(k) Number
K974432
510(k) Type
Traditional
Applicant
ULTRAGUIDE LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/9/1998
Days to Decision
77 days
Submission Type
Summary

ULTRAGUIDE 1000

Page Type
Cleared 510(K)
510(k) Number
K974432
510(k) Type
Traditional
Applicant
ULTRAGUIDE LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/9/1998
Days to Decision
77 days
Submission Type
Summary