510(k) K252677

Polyshield Safety IV Catheters by Poly Medicure Limited — Product Code FOZ

K252677 is an FDA 510(k) premarket notification submitted by Poly Medicure Limited for the device "Polyshield Safety IV Catheters". The FDA issued a decision of Substantially Equivalent on November 5, 2025. The device falls under product code FOZ (Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days), a Class II device regulated under 21 CFR 880.5200. Poly Medicure Limited has at least 5 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 5, 2025
Date Received
August 25, 2025
Clearance Type
Special
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
Device Class
Class II
Regulation Number
880.5200
Review Panel
HO
Submission Type