Last synced on 14 November 2025 at 11:06 pm

RADIUS PUSH OVER THE GUIDE WIRE PERCUTANEOUS ENDOSCOPIC GASTROSTOMY KIT

Page Type
Cleared 510(K)
510(k) Number
K972102
510(k) Type
Traditional
Applicant
RADIUS INTL., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/23/1998
Days to Decision
233 days
Submission Type
Summary

RADIUS PUSH OVER THE GUIDE WIRE PERCUTANEOUS ENDOSCOPIC GASTROSTOMY KIT

Page Type
Cleared 510(K)
510(k) Number
K972102
510(k) Type
Traditional
Applicant
RADIUS INTL., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/23/1998
Days to Decision
233 days
Submission Type
Summary