FDA 510(k) FDA class 2 Substantially Equivalent 🇬🇧 United Kingdom

CANDIDATE(R) SUPER

K Number: K863499 · Decision Mar 19, 1987
Classifications
1
FEI Numbers
2
Registration Numbers
2
Same Product Code
2
Applicant Total
17
Review Days
191

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Basic Information

Device Name
CANDIDATE(R) SUPER
K Number
K863499
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3165
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Mercia Diagnostics , Ltd.
Date Received
September 9, 1986
Decision Date
March 19, 1987
Product Code
LRF
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
LRF Candida Spp., Direct Antigen, Id

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Other Clearances by Mercia Diagnostics , Ltd.

K Number Device Name
K915479 CAPTIA CMV-TA
K904524 CAPTIA(R) SYPHILIS M, MODIFICATION
K900654 MODIFIED CAPTIA(R) SYPHILIS-M
K896295 CAPTIA(R) CMV-M
K900655 MODIFIED CAPTIA(R) TOXO-M
K896194 CAPTIA(R) CMV-G
K883924 CAPTIA(R) RUBELLA-G
K885300 CAPTIA(R) RUBELLA-M
K892802 SUPER DUO
K881425 CAPTIA(R) SYPHILIS-G
Search all 17 clearances from Mercia Diagnostics , Ltd. →