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RADIUS LOW PROFILE GASTROSTOMY TUBE KIT

Page Type
Cleared 510(K)
510(k) Number
K971901
510(k) Type
Traditional
Applicant
RADIUS INTL., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/22/1998
Days to Decision
244 days
Submission Type
Summary

RADIUS LOW PROFILE GASTROSTOMY TUBE KIT

Page Type
Cleared 510(K)
510(k) Number
K971901
510(k) Type
Traditional
Applicant
RADIUS INTL., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/22/1998
Days to Decision
244 days
Submission Type
Summary