FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

CHLAMYDELISA TEST KIT

K Number: K821967 · Decision Aug 3, 1982
Classifications
1
FEI Numbers
10
Registration Numbers
10
Same Product Code
66
Applicant Total
12
Review Days
32

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
CHLAMYDELISA TEST KIT
K Number
K821967
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.3120
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
M.A. Bioproducts
Date Received
July 2, 1982
Decision Date
August 3, 1982
Product Code
LJC
Advisory Committee
Microbiology
Review Advisory Committee
MI
Third Party
N

Classifications

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

Product Code Device Name
LJC Enzyme Linked Immunoabsorbent Assay, (Chlamydiae Group)

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (LJC), ordered by most recent decision date.

View all

Other Clearances by M.A. Bioproducts

K Number Device Name
K822883 HERPELISA KIT
K823804 MYCOPLASMELISA TEST KIT
K830045 MUMPSELISA TEST KIT
K830615 CYTOMEGELISA STAT
K823805 VARICELISA TEST KIT
K821762 MEASELISA TEST KIT
K813221 TOXOELISA TEST KIT
K812531 CELL CULTURE REAGENTS
K812123 CYTOMEGELISA TEST KIT
K802508 RUBELISA IGM TEST KIT
Search all 12 clearances from M.A. Bioproducts →