Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

VeriSafe Safety sterile syringes

K-Number: K231792 · 2023-09-28

Decision Date2023-09-28
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VeriSafe Safety sterile syringes is a medical device manufactured by Promisemed Hangzhou Meditech Co., Ltd.. It received FDA 510(k) clearance on 2023-09-28 under approval number K231792. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VeriSafe Safety sterile syringes?

VeriSafe Safety sterile syringes is a medical device that received FDA 510(k) clearance on 2023-09-28. It is manufactured by Promisemed Hangzhou Meditech Co., Ltd.. The 510(k) number is K231792.

When was VeriSafe Safety sterile syringes approved by the FDA?

VeriSafe Safety sterile syringes received FDA 510(k) clearance on 2023-09-28, under approval number K231792.

What company makes VeriSafe Safety sterile syringes?

VeriSafe Safety sterile syringes is manufactured by Promisemed Hangzhou Meditech Co., Ltd..

What is the FDA product code for VeriSafe Safety sterile syringes?

The FDA product code for VeriSafe Safety sterile syringes is FMF.

Related PubMed Literature

Other Devices by Promisemed Hangzhou Meditech Co., Ltd.

View all 35 devices →

Related Devices (Code: FMF)

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.