Verisafe Safety Retractable Insulin Syringes

FDA 510(k) K250192 · Promisemed Hangzhou Meditech Co., Ltd.

Substantially Equivalent

510(k) numberK250192

Submission

Device name
Verisafe Safety Retractable Insulin Syringes
Applicant
Promisemed Hangzhou Meditech Co., Ltd.
Hangzhou City, CN
Received
January 23, 2025
Decision date
December 10, 2025
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
FMF – Syringe, Piston
Device class
Class II (moderate risk)
Regulation
21 CFR 880.5860
Specialty
General Hospital

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Questions and answers

When was Verisafe Safety Retractable Insulin Syringes cleared by the FDA?

Verisafe Safety Retractable Insulin Syringes (K250192) received a 510(k) decision of Substantially Equivalent on December 10, 2025, 321 days after the submission was received.

What is the product code of K250192?

The FDA product code is FMF – Syringe, Piston, a Class II (moderate risk) device regulated under 21 CFR 880.5860.