HEPANOSTIKA(TM) ANTI-HAV MIDROELISA SYSTEM

FDA Premarket Approval P830018 S001

This medical device record is a pma supplement. A supplement may have changed the device description/function or indication from that approved in the original pma. Be sure to look at the original pma record for more information.

Pre-market Approval Supplement Details

DeviceHEPANOSTIKA(TM) ANTI-HAV MIDROELISA SYSTEM
Generic NameHepatitis A Test (antibody And Igm Antibody)
ApplicantORGANON TEKNIKA CORP.
Date Received1989-08-25
Decision Date1990-03-21
PMAP830018
SupplementS001
Product CodeLOL 
Advisory CommitteeMicrobiology
Supplement TypeNormal 180 Day Track
Supplement ReasonLocation Change - Manufacturer/sterilizer/packager/supplier
Expedited ReviewNo
Combination Product No
Applicant Address ORGANON TEKNIKA CORP. 100 Akzo Ave. durham, NC 27712

Supplemental Filings

Supplement NumberDateSupplement Type
P830018Original Filing
S001 1989-08-25 Normal 180 Day Track

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