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U.S. ENDOSCOPY GROUP, INC. BALLOON REPLACEMENT GASTROSTOMY TUBE

Page Type
Cleared 510(K)
510(k) Number
K955181
510(k) Type
Traditional
Applicant
UNITED STATES ENDOSCOPY GROUP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/5/1996
Days to Decision
205 days
Submission Type
Summary

U.S. ENDOSCOPY GROUP, INC. BALLOON REPLACEMENT GASTROSTOMY TUBE

Page Type
Cleared 510(K)
510(k) Number
K955181
510(k) Type
Traditional
Applicant
UNITED STATES ENDOSCOPY GROUP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/5/1996
Days to Decision
205 days
Submission Type
Summary