FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

GENETIC SYS LEGIONELLA IMMUNOFLURORES

K Number: K842683 · Decision Aug 2, 1984
Classifications
1
FEI Numbers
12
Registration Numbers
12
Same Product Code
17
Applicant Total
12
Review Days
23

Basic Information

Device Name
GENETIC SYS LEGIONELLA IMMUNOFLURORES
K Number
K842683
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3300
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
GENETIC SYSTEMS CORP.
Date Received
July 10, 1984
Decision Date
August 2, 1984
Product Code
LHL
Advisory Committee
Microbiology
Review Advisory Committee
IM
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LHL Reagents, Antibody, Legionella, Direct & Indirect Fluorescent

Similar 510(k) Clearances

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Other Clearances by GENETIC SYSTEMS CORP.

K Number Device Name
K891767 GENETIC SYSTEMS MICROPLATE READER
K891765 GENETIC SYSTEMS PIPETTOR/DILUTOR
K891768 GENETIC SYSTEMS MICROPLATE WASHER
K891766 GENETIC SYSTEMS MICROPLATE STRIP WASHER
K890768 PNEUMOCYSTIS CARINII IMMUNOFLUORESCENCE TEST KIT
K873564 GENETIC SYSTEMS RSV REAGENT CONTROL SLIDES
K873542 MICROPLATE AUTO-WASHER (MOTORIZED STAGE)
K870176 GENETIC SYSTEMS RSV IMMUNOFLUORESCENCE TEST KIT
K870879 ALANINE TRANSAMINASE (ALT) TEST KIT
K863566 GSC 1000
Search all 12 clearances from GENETIC SYSTEMS CORP. →