DHI — Ng3m(Bo), Antigen, Antiserum, Control Class I

FDA Device Classification

FDA product code DHI covers "Ng3m(Bo), Antigen, Antiserum, Control", a Class I medical device regulated under 21 CFR 866.5065. Submissions are reviewed by the Immunology panel. At least 1 recent 510(k) clearance has been granted under this product code.

Classification Details

Product Code
DHI
Device Class
Class I
Regulation Number
866.5065
Submission Type
Review Panel
IM
Medical Specialty
Immunology
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K810625serono laboratoriesHUMAN PLACENTAL LACTOGEN RADIOIMMUNO-March 27, 1981