510(k) K781644

Device
ANTIBIOTIC NEPHELOMETER
Applicant
BIOVATION, INC.
510(k) number
K781644
Product code
JQX  
Decision
Substantially Equivalent (SESE)
Decision date
1978-10-03
Date received
1978-09-25
Regulation
862.2700
Classification name
Nephelometer, For Clinical Use
Medical specialty
Clinical Chemistry
Review panel
Microbiology
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 JQX  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K962294IMMAGE IMMUNOCHEMISTRY SYSTEMBeckman Instruments, Inc.1996-08-21
K922273ARRAY(R) 360Beckman Instruments, Inc.1992-08-19
K885263QMS(TM) - THEOPHYLLINESeradyn, Inc.1989-03-28
K851253TDX ANALYZER W/NEPHELOMETRY CAROUSELAbbott Laboratories1985-04-30
K851234A-JUST TURBIDITY METERAbbott Laboratories1985-04-29
K801362ALBUMIN NEPHELOMETRIC ASSAYJ.T. Baker Chemical Co.1980-07-21
K801089J.T. BAKER NEPHELOMETERJ.T. Baker Chemical Co.1980-05-28
K792045BIOVATION NEPHELOMETERBiovation, Inc.1979-10-30
K790103NEPHELOMETER, MIC-2000 LASERDynatech Corp.1979-03-12
K781554RAD-291Organon, Inc.1978-10-11
K780251NEPHELOMETERKallestad Laboratories, Inc.1978-04-06
K772361LASER IMMUNONEPHELOMETRIC ANALYZERG.D. Searle and Co.1978-01-30
K771446TRANSPORTEO MODULEHyland Therapeutic Div., Travenol Laboratories1977-08-10

Legacy Summary#

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FDA Review#

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