Last synced on 14 November 2025 at 11:06 pm

Single Use Preloaded Sphincterotome V (Distal Wire Guided) (KD-VC600 Series); Single Use Sphincterotome V (Distal Wire Guided) (KD-VC400 Series); Single Use 3-Lumen Sphincterotome (KD-V Series); Disposable Triple Lumen Sphincterotome (KD Series)

Page Type
Cleared 510(K)
510(k) Number
K250945
510(k) Type
Traditional
Applicant
Olympus Medical Systems Corp.
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
10/17/2025
Days to Decision
203 days
Submission Type
Summary

Single Use Preloaded Sphincterotome V (Distal Wire Guided) (KD-VC600 Series); Single Use Sphincterotome V (Distal Wire Guided) (KD-VC400 Series); Single Use 3-Lumen Sphincterotome (KD-V Series); Disposable Triple Lumen Sphincterotome (KD Series)

Page Type
Cleared 510(K)
510(k) Number
K250945
510(k) Type
Traditional
Applicant
Olympus Medical Systems Corp.
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
10/17/2025
Days to Decision
203 days
Submission Type
Summary