510(k) K944738

Device
Series 600 Centrifuge-four Separate Variations Of The Same Base Centrifuge
Applicant
DUCKER CL
510(k) number
K944738
Product code
JQC
Decision
Substantially Equivalent (SESE)
Decision date
1994-10-19
Date received
1994-09-26
Regulation
862.2050
Classification name
Centrifuges (Micro, Ultra, Refrigerated) For Clinical Use
Medical specialty
Clinical Chemistry
Review panel
Clinical Chemistry
Device class
1
Clearance type
Traditional
Statement or summary
Statement
Third party reviewed
No

Applicant Contact#

Contact
KENNETH J MOSCONE
Address
4507 NW 103rd Ave. Sunrise FL US 33351 33351

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

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