AMIKACIN ELUTION DISK FOR AUTOBAC

FDA Premarket Approval N50485 S005

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

DeviceAMIKACIN ELUTION DISK FOR AUTOBAC
Generic NameDiscs, Elution
ApplicantORGANON TEKNIKA CORP.
Date Received1981-12-01
Decision Date1982-08-06
PMAN50485
SupplementS005
Product CodeLTX 
Advisory CommitteeMicrobiology
Expedited ReviewNo
Combination Product No
Applicant Address ORGANON TEKNIKA CORP. 800 Capitola Dr. durham, NC 27713

Supplemental Filings

Supplement NumberDateSupplement Type
N50485Original Filing
S017 1987-10-07 Normal 180 Day Track
S016 1987-06-12 Normal 180 Day Track
S015 1987-04-22 Normal 180 Day Track
S014 1984-08-16
S013 1984-04-23 Normal 180 Day Track
S012 1984-04-23 Normal 180 Day Track
S011 1984-03-02
S010 1984-01-05
S009 1983-12-08
S008
S007 1983-09-13
S006 1983-07-26
S005 1981-12-01
S004
S003 1980-08-12
S002 1979-10-29
S001 1979-10-22

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