FDA.reportPublic FDA data

510(k) K822078

Device
Dade Disp. Dispensing-spreading Pipets
Applicant
AMERICAN DADE
510(k) number
K822078
Product code
JRC
Decision
Substantially Equivalent (SESE)
Decision date
1982-07-27
Date received
1982-07-15
Regulation
862.2050
Classification name
Micro Pipette
Medical specialty
Clinical Chemistry
Review panel
Clinical Chemistry
Device class
1
Clearance type
Traditional
Third party reviewed
No

Applicant Contact#

Address
4221 Richmond Rd., NW Walker MI US 49534 49534

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code JRC#

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K840186SMI DIGITRONScientific Manufacturing Industries1984-04-05
K834100PRE-CALIBRATED PIPETTESVitex1984-02-21
K792696MICROPITETTEMeridian Diagnostics, Inc.1980-02-01
K770594LABORATORY EXPENDABLE PRODUCTSAbco Dealers, Inc.1977-07-06
K760621LANCER PLASTIC TRANSFER PIPETTESherwood Medical Industries1976-10-05