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RADIUS PULL PERCUTANEOUS ENDOSCOPIC GASTROSTOMY KIT

Page Type
Cleared 510(K)
510(k) Number
K972025
510(k) Type
Traditional
Applicant
Radius Intl., Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/23/1998
Days to Decision
235 days
Submission Type
Summary

RADIUS PULL PERCUTANEOUS ENDOSCOPIC GASTROSTOMY KIT

Page Type
Cleared 510(K)
510(k) Number
K972025
510(k) Type
Traditional
Applicant
Radius Intl., Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/23/1998
Days to Decision
235 days
Submission Type
Summary