510(k) K251877

JMS CAVEO A.V. Fistula Needle Set by JMS North America Corporation — Product Code FIE

K251877 is an FDA 510(k) premarket notification submitted by JMS North America Corporation for the device "JMS CAVEO A.V. Fistula Needle Set". The FDA issued a decision of Substantially Equivalent on August 15, 2025. The device falls under product code FIE (Needle, Fistula), a Class II device regulated under 21 CFR 876.5540. JMS North America Corporation has at least 8 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 15, 2025
Date Received
June 18, 2025
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Needle, Fistula
Device Class
Class II
Regulation Number
876.5540
Review Panel
GU
Submission Type