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Plasma Processing System For Converting Alpha To Pre-Beta High-Density Lipoprotein

Page Type
Product Code
Definition
To reduce coronary atheroma in patients with Homozygous Familial Hypercholesterolemia.
Physical State
Automated plasma processing system, system accessories, and solutions.
Technical Method
Off-line plasma processing system that mixes blood plasma with delipidation solutions for converting alpha to pre-beta high-density lipoprotein.
Target Area
Blood plasma.
Review Panel
Gastroenterology and Urology
Submission Type
HDE - Humanitarian Device Exemption
Device Classification
F
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

The FDA has not linked product code QNB to any particular section of the CFR (Code of Federal Regulations). There are multiple reasons why this might be the case:

  • The product code was created for a class III submission that does not follow the normal PMN or PMA path - e.g., for a device that falls under HDE (Humanitarian Device Exemption) or EUA (Emergency Use Authorization).
  • The FDA has generated the product code for an existing Class III device, as a result of a PMA supplement that modifies the device in a way that it can't fit under the existing product code originally assigned
  • The product code was created for internal use at the FDA, and not for classification or regulatory-related purposes.

Plasma Processing System For Converting Alpha To Pre-Beta High-Density Lipoprotein

Page Type
Product Code
Definition
To reduce coronary atheroma in patients with Homozygous Familial Hypercholesterolemia.
Physical State
Automated plasma processing system, system accessories, and solutions.
Technical Method
Off-line plasma processing system that mixes blood plasma with delipidation solutions for converting alpha to pre-beta high-density lipoprotein.
Target Area
Blood plasma.
Review Panel
Gastroenterology and Urology
Submission Type
HDE - Humanitarian Device Exemption
Device Classification
F
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

The FDA has not linked product code QNB to any particular section of the CFR (Code of Federal Regulations). There are multiple reasons why this might be the case:

  • The product code was created for a class III submission that does not follow the normal PMN or PMA path - e.g., for a device that falls under HDE (Humanitarian Device Exemption) or EUA (Emergency Use Authorization).
  • The FDA has generated the product code for an existing Class III device, as a result of a PMA supplement that modifies the device in a way that it can't fit under the existing product code originally assigned
  • The product code was created for internal use at the FDA, and not for classification or regulatory-related purposes.