Immuno-Wash Automated Tube Washer

FDA 510(k) K893810 · Ocean Scientific, Inc.

Substantially Equivalent

510(k) numberK893810

Submission

Device name
Immuno-Wash Automated Tube Washer
Applicant
Ocean Scientific, Inc.
Garden Grove, CA, US
Received
May 22, 1989
Decision date
August 3, 1989
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JQW – Station, Pipetting And Diluting, For Clinical Use
Device class
Class I (low risk)
Regulation
21 CFR 862.2750
Specialty
Clinical Chemistry

Other 510(k)s with product code JQW

510(k)DeviceApplicantDecision
K023955BD Viper InstrumentJQW · Traditional Becton, Dickinson & CO06/24/2003SE
K973335Quatro SP Sample Processing Systems (200-499, Inclusive)JQW · Traditional Zenyx Scientific , Ltd.04/30/1998SE
K9801802700 Sample ManagerJQW · Traditional Waters Corporation02/12/1998SE
K970420Mastercap Am 5.0/MASTERCAP RM 5.0JQW · Traditional Pharmacia, Inc.06/30/1997SE
K970616Mini Sampler ProcessorJQW · Traditional Cavro Scientific Instruments, Inc.04/21/1997SE
K962687Gio. de Vita E C. S.R.L.(Gdv) Automatic Washing SystemJQW · Traditional Nichols Institute Diagnostics03/28/1997SE
K962859Mini Sample ProcessorJQW · Traditional Cavro Scientific Instruments, Inc.10/29/1996SE
K961896Microlab 4000, Microlab 4200JQW · Traditional Hamilton Co.08/16/1996SE
K961694ImpactJQW · Traditional Matrix Technologies Corp.06/21/1996SE
K953345GenesisJQW · Traditional Tecan U.S., Inc.11/21/1995SE

More from Tecan U.S., Inc.

510(k)DeviceDecision
K873638Micro-Chem AnalyzerJJQ · Traditional 09/29/1987SE
K864731Ocean Scientific VDRL TestGMQ · Traditional 03/10/1987SE
K863976Ocean Scientific VacutestJKA · Traditional 10/24/1986SE
K860987Mini-Chem AnalyzerJJQ · Traditional 05/05/1986SE
K840340Chem-Stat AnalyzerJJQ · Traditional 03/23/1984SE

Questions and answers

When was Immuno-Wash Automated Tube Washer cleared by the FDA?

Immuno-Wash Automated Tube Washer (K893810) received a 510(k) decision of Substantially Equivalent on August 3, 1989, 73 days after the submission was received.

What is the product code of K893810?

The FDA product code is JQW – Station, Pipetting And Diluting, For Clinical Use, a Class I (low risk) device regulated under 21 CFR 862.2750.