Novapath SP Advanced Liquid Handling System

FDA 510(k) K900775 · Bio-Rad

Substantially Equivalent

510(k) numberK900775

Submission

Device name
Novapath SP Advanced Liquid Handling System
Applicant
Bio-Rad
Hercules, CA, US
Received
February 20, 1990
Decision date
March 9, 1990
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

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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

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Questions and answers

When was Novapath SP Advanced Liquid Handling System cleared by the FDA?

Novapath SP Advanced Liquid Handling System (K900775) received a 510(k) decision of Substantially Equivalent on March 9, 1990, 17 days after the submission was received.

What is the product code of K900775?

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.