Cleared Traditional

TK Intravascular Administration Set

K191640 · Anhui Tiankang Medical Technology Co., Ltd. · General Hospital
Aug 2020
Decision
434d
Days
Class 2
Risk

About This 510(k) Submission

K191640 is an FDA 510(k) clearance for the TK Intravascular Administration Set, a Set, Administration, Intravascular (Class II — Special Controls, product code FPA), submitted by Anhui Tiankang Medical Technology Co., Ltd. (Tianchang, CN). The FDA issued a Cleared decision on August 26, 2020, 434 days after receiving the submission on June 19, 2019. This device falls under the General Hospital review panel. Regulated under 21 CFR 880.5440.

Submission Details

510(k) Number K191640 FDA.gov
FDA Decision Cleared SESE
Date Received June 19, 2019
Decision Date August 26, 2020
Days to Decision 434 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary Summary PDF

Device Classification

Product Code FPA — Set, Administration, Intravascular
Device Class Class II — Special Controls
CFR Regulation 21 CFR 880.5440

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