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

DIASTAT ANTI-CARDIOLIPIN IGG/IGM, MODEL FCAR 600

K Number: K001574 · Decision Jun 9, 2000
Classifications
1
FEI Numbers
25
Registration Numbers
25
Same Product Code
93
Applicant Total
1
Review Days
18

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
DIASTAT ANTI-CARDIOLIPIN IGG/IGM, MODEL FCAR 600
K Number
K001574
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5660
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Axis-Shield
Date Received
May 22, 2000
Decision Date
June 9, 2000
Product Code
MID
Advisory Committee
Immunology
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
MID System, Test, Anticardiolipin Immunological

Similar 510(k) Clearances

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

View all