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

MODIFIED CAPTIA(R) SYPHILIS-M

K Number: K900654 · Decision Mar 8, 1990
Classifications
1
FEI Numbers
27
Registration Numbers
27
Same Product Code
34
Applicant Total
17
Review Days
27

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
MODIFIED CAPTIA(R) SYPHILIS-M
K Number
K900654
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3830
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Mercia Diagnostics , Ltd.
Date Received
February 9, 1990
Decision Date
March 8, 1990
Product Code
LIP
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
LIP Enzyme Linked Immunoabsorption Assay, Treponema Pallidum

Similar 510(k) Clearances

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

View all

Other Clearances by Mercia Diagnostics , Ltd.

K Number Device Name
K915479 CAPTIA CMV-TA
K904524 CAPTIA(R) SYPHILIS M, MODIFICATION
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
K880918 CAPTIA TOXO-G
Search all 17 clearances from Mercia Diagnostics , Ltd. →