Last synced on 27 March 2026 at 11:12 pm

Non-Factor Replacement Product Test System

Page Type
Product Code
Definition
A non-factor replacement product test system is a prescription in vitro diagnostic device intended to measure non-factor replacement therapeutic products that are indicated for routine prophylaxis to prevent or reduce the frequency of bleeding episodes in patients with bleeding disorders, including hemophilia, in human blood specimens to ensure appropriate therapy in accordance with the approved non-factor replacement product labeling.
Physical State
In vitro diagnostic device
Technical Method
Qualitative and quantitative detection of non-factor replacement product
Target Area
Human blood specimen
Regulation Medical Specialty
Hematology
Review Panel
Hematology
Submission Type
510(K)
Device Classification
Class 2
Regulation Number
864.7298
GMP Exempt?
No
Summary Malfunction Reporting
Ineligible
Implanted Device
No
Life-Sustain/Support Device
No
Third Party Review
Not Third Party Eligible

No Linked CFR Text

Product code SES is linked to regulation 21CFR864.7298, which does not seem to exist yet. It may be pending at the moment.

Non-Factor Replacement Product Test System

Page Type
Product Code
Definition
A non-factor replacement product test system is a prescription in vitro diagnostic device intended to measure non-factor replacement therapeutic products that are indicated for routine prophylaxis to prevent or reduce the frequency of bleeding episodes in patients with bleeding disorders, including hemophilia, in human blood specimens to ensure appropriate therapy in accordance with the approved non-factor replacement product labeling.
Physical State
In vitro diagnostic device
Technical Method
Qualitative and quantitative detection of non-factor replacement product
Target Area
Human blood specimen
Regulation Medical Specialty
Hematology
Review Panel
Hematology
Submission Type
510(K)
Device Classification
Class 2
Regulation Number
864.7298
GMP Exempt?
No
Summary Malfunction Reporting
Ineligible
Implanted Device
No
Life-Sustain/Support Device
No
Third Party Review
Not Third Party Eligible

No Linked CFR Text

Product code SES is linked to regulation 21CFR864.7298, which does not seem to exist yet. It may be pending at the moment.