Microlab M-Microprocessor Diluter/Disp

FDA 510(k) K801913 · Hamilton Co.

Substantially Equivalent

510(k) numberK801913

Submission

Device name
Microlab M-Microprocessor Diluter/Disp
Applicant
Hamilton Co.
Mchenry, IL, US
Received
August 11, 1980
Decision date
September 26, 1980
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
K961896Microlab 4000, Microlab 4200JQW · Traditional 08/16/1996SE
K943493Discrete Photometric Chemistry AnalyzerJJE · Traditional 01/30/1995SE
K892369Multi-Probe Head PlusJTC · Traditional 06/02/1989SE
K873893LumiconJJQ · Traditional 01/05/1988SE
K871945Microlab atJTC · Traditional 05/29/1987SE
K832205Precision Liquid DispenserJQW · Traditional 08/24/1983SE
K832204Microlab PJQW · Traditional 08/24/1983SE
K832202PB 600 Repeating DispenserJQW · Traditional 08/24/1983SE
K832201Chrom-PrepKZR · Traditional 08/16/1983SE
K832200PRP-1 Reversed Phase Columns for HPLCDPM · Traditional 08/16/1983SE

Questions and answers

When was Microlab M-Microprocessor Diluter/Disp cleared by the FDA?

Microlab M-Microprocessor Diluter/Disp (K801913) received a 510(k) decision of Substantially Equivalent on September 26, 1980, 46 days after the submission was received.

What is the product code of K801913?

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.