FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Access OV Monitor

K Number: K240479 · Decision May 10, 2024
Classifications
1
FEI Numbers
30
Registration Numbers
30
Same Product Code
25
Applicant Total
17
Review Days
80

Basic Information

Device Name
Access OV Monitor
K Number
K240479
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.6010
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Beckman Coulter, Inc
Date Received
February 20, 2024
Decision Date
May 10, 2024
Product Code
LTK
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
LTK Test, Epithelial Ovarian Tumor-Associated Antigen (Ca125)

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