Dispenser Aspirator Da 300

FDA 510(k) K812782 · Pharmacia, Inc.

Substantially Equivalent

510(k) numberK812782

Submission

Device name
Dispenser Aspirator Da 300
Applicant
Pharmacia, Inc.
Mchenry, IL, US
Received
October 5, 1981
Decision date
October 23, 1981
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
K974350Allergan Immuno Cap M4, M8, K70DHB · Traditional 02/09/1998SE
K972364Unicap PhadiatopDHB · Traditional 09/04/1997SE
K972068Unicap Specific Ige Feia Assay, Latex Allergen Immunocap K82DHB · Traditional 07/03/1997SE
K970420Mastercap Am 5.0/MASTERCAP RM 5.0JQW · Traditional 06/30/1997SE
K964152Unicap Total Ige Assay/Pharmacia Total Ige Controls LMHDGC · Traditional 04/23/1997SE
K962274Unicap 100DHB · Traditional 09/12/1996SE
K941993Pharmacia Cap System Phadiatop FeiaDHB · Traditional 01/30/1996SE
K954337Genotropin MixerFMF · Traditional 11/13/1995SE
K951025Piston SyringeFMF · Traditional 10/19/1995SE
K952025RobocapJQW · Traditional 07/26/1995SE

Questions and answers

When was Dispenser Aspirator Da 300 cleared by the FDA?

Dispenser Aspirator Da 300 (K812782) received a 510(k) decision of Substantially Equivalent on October 23, 1981, 18 days after the submission was received.

What is the product code of K812782?

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.