TK Safety Needle
K-Number: K191644 · 2020-08-06
Device Summary
Frequently Asked Questions
What is the TK Safety Needle?
TK Safety Needle is a medical device that received FDA 510(k) clearance on 2020-08-06. The listed applicant is Anhui Tiankang Medical Technology Co., Ltd.. The 510(k) number is K191644.
When did TK Safety Needle receive FDA 510(k) clearance?
TK Safety Needle received FDA 510(k) clearance on 2020-08-06, under 510(k) number K191644.
Who is the listed applicant for TK Safety Needle?
The FDA 510(k) record lists Anhui Tiankang Medical Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TK Safety Needle?
The FDA product code for TK Safety Needle is FMI.
Other records listing Anhui Tiankang Medical Technology 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: FMI)
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.