Cleared Traditional

K991120 - VACUTAINER BRAND CTAD TUBE (MULTIPLE)

K991120 is an FDA 510(k) clearance for VACUTAINER BRAND CTAD TUBE (MULTIPLE), manufactured by Becton Dickinson Vacutainer Systems. The device is a Class 2 Chemistry device with product code JKA cleared through the Traditional 510(k) pathway after a 47-day FDA review.

K991120 · Becton Dickinson Vacutainer Systems · Chemistry device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
May 1999
Decision
47d
Days
Class 2
Risk

K991120 is an FDA 510(k) clearance for the VACUTAINER BRAND CTAD TUBE (MULTIPLE). Classified as Tubes, Vials, Systems, Serum Separators, Blood Collection (product code JKA), Class II - Special Controls.

Submitted by Becton Dickinson Vacutainer Systems (Franklin Lakes, US). The FDA issued a Cleared decision on May 19, 1999 after a review of 47 days - a notably fast clearance cycle.

This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.1675 - the FDA in vitro diagnostics and chemistry framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Becton Dickinson Vacutainer Systems devices

FDA 510(k) Submission Details - K991120

510(k) Number K991120 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 02, 1999
Decision Date May 19, 1999
Days to Decision 47 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
41d faster than avg
Panel avg: 88d · This submission: 47d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

JKA Device Classification - Class 2, Special Controls

Product Code JKA Tubes, Vials, Systems, Serum Separators, Blood Collection
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 862.1675
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Chemistry devices follow this clearance model.

Regulatory Peers - JKA Tubes, Vials, Systems, Serum Separators, Blood Collection

All 164
Devices cleared under the same product code (JKA) and FDA review panel - the closest regulatory comparables to K991120.
GREINER MINICOLLECT COAGULATION BLOOD COLLECTION TUBE
K992244 · Greiner Meditech, Inc. · Jul 1999
GREINER MINICOLLECT LITHIUM HEPARIN GEL BLOOD COLLECTION TUBE
K991843 · Greiner Meditech, Inc. · Jun 1999
VACUTAINER BRAND MULTIPLE SAMPLE LUER ADAPTER, BLOOD COLLECTION SETS AND SAFETY-LOK BLOOD COLLECTION, SAFETY BLOOD COLLE
K991088 · Becton Dickinson Vacutainer Systems · May 1999
GREINER VACUETTE BLOOD COLLECTION TUBE
K983952 · Greiner Meditech, Inc. · Dec 1998
TERUMO VENOJECT,LUER ADAPTER
K983490 · Terumo Corp. · Nov 1998
SAFE-T-FILL CAPILLARY BLOOD COLLECTION SYSTEM
K983517 · Ram Scientific · Nov 1998