Anti-Glutamate Receptor (Type Nmda) Ifa
FDA product code OSK · 1 cleared devices
- Regulation
- 21 CFR 866.5660
- Review panel
- IM
- Implant
- No
- Life sustaining
- No
- Third party review
- Yes
- GMP exempt
- No
- Clearance span
- 2010-09-13 – 2010-09-13
Intended for the qualitative determination of autoantibodies against glutamate receptor (type NMDA) in human serum. Used as an aid in the diagnosis of anti-glutamate receptor (type NMDA) autoimmune encephalitis in conjunction with other laboratory and clinical findings.
No matching devices.
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