510(k) K250949

Suction Valve (MAJ-1443); Air/Water Valve (MAJ-1444) by Olympus Medical Systems Corporation — Product Code ODC

K250949 is an FDA 510(k) premarket notification submitted by Olympus Medical Systems Corporation for the device "Suction Valve (MAJ-1443); Air/Water Valve (MAJ-1444)". The FDA issued a decision of Substantially Equivalent on July 16, 2025. The device falls under product code ODC (Endoscope Channel Accessory), a Class II device regulated under 21 CFR 876.1500. Olympus Medical Systems Corporation has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 16, 2025
Date Received
March 28, 2025
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Endoscope Channel Accessory
Device Class
Class II
Regulation Number
876.1500
Review Panel
GU
Submission Type

To give the endoscope channel additional or improved functionality.