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LF-DP GASTROINTESTINAL AND SIGMOID FIBERSCOPE, ACCESSORIES AND ANCILLARY EQUIPMENT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K002231
510(k) Type
Traditional
Applicant
Olympus Optical Co., Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/30/2001
Days to Decision
190 days
Submission Type
Summary

LF-DP GASTROINTESTINAL AND SIGMOID FIBERSCOPE, ACCESSORIES AND ANCILLARY EQUIPMENT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K002231
510(k) Type
Traditional
Applicant
Olympus Optical Co., Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/30/2001
Days to Decision
190 days
Submission Type
Summary