510(k) K250192

Verisafe Safety Retractable Insulin Syringes by Promisemed Hangzhou Meditech Co., Ltd. — Product Code FMF

K250192 is an FDA 510(k) premarket notification submitted by Promisemed Hangzhou Meditech Co., Ltd. for the device "Verisafe Safety Retractable Insulin Syringes". The FDA issued a decision of Substantially Equivalent on December 10, 2025. The device falls under product code FMF (Syringe, Piston), a Class II device regulated under 21 CFR 880.5860. Promisemed Hangzhou Meditech Co., Ltd. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 10, 2025
Date Received
January 23, 2025
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Syringe, Piston
Device Class
Class II
Regulation Number
880.5860
Review Panel
HO
Submission Type