FDA 510(k) FDA class 1 Substantially Equivalent 🇬🇧 United Kingdom

IDEIA(TM) CHLAMYDIA BLOCKING REAGENTS, MODIFICATION

K Number: K940564 · Decision Jan 11, 1996
Classifications
1
FEI Numbers
10
Registration Numbers
10
Same Product Code
66
Applicant Total
6
Review Days
707

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Basic Information

Device Name
IDEIA(TM) CHLAMYDIA BLOCKING REAGENTS, MODIFICATION
K Number
K940564
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.3120
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Dako Diagnostics , Ltd.
Date Received
February 3, 1994
Decision Date
January 11, 1996
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.

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Other Clearances by Dako Diagnostics , Ltd.

K Number Device Name
K981226 IMAGEARAINFLUENZA VIRUS GROUP (TYPES 1,2 AND 3) TEST AND IMAGEN PARAINFLUENZA VIRUS TEST TYPES 1,2 AND 3
K973954 IMAGEN RESPIRATORY SCREEN
K962037 IMAGEN RESPIRATORY SCREEN
K943557 IMAGEN
K932384 IDEIA(TM) ROTAVIRUS