510(k) K000844

Device
ABSOLUTE HCG PREGNANCY TEST
Applicant
MIZUHO USA, INC.
510(k) number
K000844
Product code
DHA  
Decision
Substantially Equivalent (SESE)
Decision date
2000-06-16
Date received
2000-03-15
Regulation
862.1155
Classification name
System, Test, Human Chorionic Gonadotropin
Medical specialty
Clinical Chemistry
Review panel
Clinical Chemistry
Device class
2
Clearance type
Traditional
Statement or summary
Statement
Third party reviewed
No

Related Records

Applicant Contact

Contact
BENEDICT ZIN
Address
6730 Mesa Ridge Rd., Suite D San Diego CA US 92121 92121

FDA Registration Numbers

Source Documents

510(k) summary PDF not indicated by FDA

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K170317Alinity i Total ß-hCG Reagent Kit, Alinity i SystemAbbott Laboratories2017-10-23
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K133002i-STAT Total beta-hCG Test, i-STAT Total beta-hCG Controls, i-STAT Total beta-hCG Calibration Verification MaterialsAbbott Point of Care, Inc.2015-04-16
K130020ACCESS TOTAL BHCG (5TH IS)Beckman Coulter, Inc.2013-10-01
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Legacy Summary

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FDA Review

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