510(k) K780341

Device
SCINTILLATION, LIQUID, RACKBETA
Applicant
LKB INSTRUMENTS, INC.
510(k) number
K780341
Product code
JJJ  
Decision
Substantially Equivalent (SESE)
Decision date
1978-05-26
Date received
1978-03-01
Regulation
862.2320
Classification name
Counter (beta, Gamma) For Clinical Use
Medical specialty
Clinical Chemistry
Review panel
Radiology
Device class
1
Clearance type
Traditional
Third party reviewed
No

Applicant Contact#

Address
803 N. Front St. Suite 3 Mchenry IL US 60050 60050

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code JJJ  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K962762SEQUENTIAL SAMPLE MULTI-PHOTON DETECTORBiotraces, Inc.1996-08-16
K946387CAPRA (CAPRAC-R) WIPETEST AND WELL COUNTERCapintec, Inc.1995-03-30
K920559ABBOTT VERTEX ANALYZERAbbott Laboratories1992-03-19
K900087GENESYS 6000 GAMMA COUNTERLaboratory Technologies, Inc.1990-07-19
K896202MATRIX(TM)-96Canberra Industries, Inc.1990-01-02
K894902SOURCEREROakfield Instruments, Ltd.1989-10-17
K884091SOURCERERJohn Caunt Scientific , Ltd.1989-02-02
K884269SAMPLE IDENTIFICATION STATION MODEL 38010Icn Micromedic Systems1989-01-09
K8740941205 BETAPLATE LIQUID SCINTILLATION COUNTERLkb Instruments, Inc.1987-11-04
K872430ISO-DATA 500 SERIES GAMMA COUNTERIso-Data, Inc.1987-08-21
K872429ISO-DATA 100 SERIES GAMMA COUNTERIso-Data, Inc.1987-08-21
K870115BERTHOLD LB 2103,2104-XT/PC/AT,951G GAMMA COUNTERSBerthold Analytical Instruments, Inc.1987-03-31
K862206TAURUS (TM) AUTOMATIC LIQUID SCINTILLATION COUNTERMicromedic Systems1986-08-04
K851164DENTOCULT CULTURE-PADDLEOrion Corp.1985-10-29
K851689GENESYS GAMMA COUNTERLaboratory Technologies, Inc.1985-08-07

Legacy Summary#

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FDA Review#

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