ANTI-LEU-4 Fitc Lysin C Buffer

FDA 510(k) K842218 · Bd Becton Dickinson Vacutainer Systems Preanalytic

Substantially Equivalent

510(k) numberK842218

Submission

Device name
ANTI-LEU-4 Fitc Lysin C Buffer
Applicant
Bd Becton Dickinson Vacutainer Systems Preanalytic
Washington, DC, US
Received
June 4, 1984
Decision date
December 27, 1984
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
LIZ – Assay, T Lymphocyte Surface Marker
Device class
Class II (moderate risk)
Regulation
21 CFR 864.5220
Specialty
Hematology

Other 510(k)s with product code LIZ

510(k)DeviceApplicantDecision
K914847CD8 Monoclonal AntibodiesLIZ · Traditional Gen Trak, Inc.06/19/1992SE
K860830Technicon H.1 System, T Lymphocytes MethodLIZ · Traditional Technicon Instruments Corp.09/08/1986SN
K843062Tbm-Reagent for T,B Cell & MonocytesLIZ · Traditional Bd Becton Dickinson Vacutainer Systems Preanalytic04/03/1985SE
K833929White Blood Cells Human Tand BLIZ · Traditional Control Diagnostics02/03/1984SE
K831053Quantigen T & B Cell AssayLIZ · Traditional Bio-Rad08/08/1983SE
K820643Ortho Spectrum III & Ortho-Mune OkLIZ · Traditional Ortho Diagnostic Systems, Inc.07/14/1982SE

More from Ortho Diagnostic Systems, Inc.

510(k)DeviceDecision
K003062Bactec Mgit 960 Sir KitsMJA · Traditional 06/06/2001SE
K0035530.9% Sodium Chloride Injection, Usp BD Pre-Filled Flush SyringeFOZ · Traditional 03/21/2001SE
K003461BD Vacutainer Passive Shielding Blood Collection NeedleFMI · Traditional 02/01/2001SE
K002938B-D Ultra-Fine III Pen Needle; Model 31G X 3/16FMI · Traditional 11/29/2000SE
K001364BD Directigen Flu A+BPSZ · Traditional 06/28/2000SE
K000762Moxifloxacin, 5 Ug, BBL Sensi-DiscJTN · Traditional 04/25/2000SE
K000829Gatifloxacin, 5 Ug, BBL Sensi-DiscJTN · Traditional 04/13/2000SE
K993186Synercid, 15 Ug, BBL Sensi-DiscJTN · Traditional 11/03/1999SE
K992734Becton Dickinson SyringeMEG · Traditional 10/01/1999SE
K992849QBC Star Centrifugal Hematology SystemGKZ · Special 09/23/1999SE

Questions and answers

When was ANTI-LEU-4 Fitc Lysin C Buffer cleared by the FDA?

ANTI-LEU-4 Fitc Lysin C Buffer (K842218) received a 510(k) decision of Substantially Equivalent on December 27, 1984, 206 days after the submission was received.

What is the product code of K842218?

The FDA product code is LIZ – Assay, T Lymphocyte Surface Marker, a Class II (moderate risk) device regulated under 21 CFR 864.5220.