Cleared Traditional

VACU LAB PLAIN TUBE, VACU LAB GEL & CLOT ACTIVATOR TUBE, VACU LAB COAGULATION TUBE

K060364 · Teco Diagnostics · Chemistry
Jun 2006
Decision
122d
Days
Class 2
Risk

About This 510(k) Submission

K060364 is an FDA 510(k) clearance for the VACU LAB PLAIN TUBE, VACU LAB GEL & CLOT ACTIVATOR TUBE, VACU LAB COAGULATION TUBE, a Tubes, Vials, Systems, Serum Separators, Blood Collection (Class II — Special Controls, product code JKA), submitted by Teco Diagnostics (Anaheim, US). The FDA issued a Cleared decision on June 15, 2006, 122 days after receiving the submission on February 13, 2006. This device falls under the Chemistry review panel. Regulated under 21 CFR 862.1675.

Submission Details

510(k) Number K060364 FDA.gov
FDA Decision Cleared SESE
Date Received February 13, 2006
Decision Date June 15, 2006
Days to Decision 122 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary Summary PDF

Device Classification

Product Code JKA — Tubes, Vials, Systems, Serum Separators, Blood Collection
Device Class Class II — Special Controls
CFR Regulation 21 CFR 862.1675

Similar Devices — JKA Tubes, Vials, Systems, Serum Separators, Blood Collection

All 232
BD Vacutainer? Plasma Separator Tubes (PST?), BD Vacutainer? Sodium Heparin Blood Collection Tubes
K252040 · Becton, Dickinson and Company · Mar 2026
Steripath? Flow? Blood Collection System
K251812 · Magnolia Medical Technologies · Sep 2025
BD Vacutainer? Eclipse? Blood Collection Needle
K243207 · Becton, Dickinson and Company · Jul 2025
Blood collection tube holders
K250961 · Promisemed Hangzhou Meditech Co., Ltd. · Jun 2025
Navi? Needle-free Blood Collection Device (VNC20500FG, VNC22500FG, VNC24500FG)
K244047 · Venocare, Inc. · May 2025
Sol-Guard TM XtraThin Safety Pull-Button Blood Collection Set
K250907 · Sol-Millennium Medical, Inc. · Apr 2025