VeriSafe Safety sterile syringes
K-Number: K231792 · 2023-09-28
Device Summary
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. The listed applicant is Promisemed Hangzhou Meditech Co., Ltd.. The 510(k) number is K231792.
When did VeriSafe Safety sterile syringes receive FDA 510(k) clearance?
VeriSafe Safety sterile syringes received FDA 510(k) clearance on 2023-09-28, under 510(k) number K231792.
Who is the listed applicant for VeriSafe Safety sterile syringes?
The FDA 510(k) record lists Promisemed Hangzhou Meditech Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VeriSafe Safety sterile syringes?
The FDA product code for VeriSafe Safety sterile syringes is FMF.
Other records listing Promisemed Hangzhou Meditech Co., Ltd. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: FMF)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.