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FUJINON DOUBLE BALLOON ENTEROSCOPY SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K040048
510(k) Type
Traditional
Applicant
FUJINON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/7/2004
Days to Decision
147 days
Submission Type
Summary

FUJINON DOUBLE BALLOON ENTEROSCOPY SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K040048
510(k) Type
Traditional
Applicant
FUJINON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/7/2004
Days to Decision
147 days
Submission Type
Summary