KLH — Antisera, C. Acnes Class I

FDA Device Classification

FDA product code KLH covers "Antisera, C. Acnes", a Class I medical device regulated under 21 CFR 866.3140. Submissions are reviewed by the Microbiology panel. At least 1 recent 510(k) clearance has been granted under this product code.

Classification Details

Product Code
KLH
Device Class
Class I
Regulation Number
866.3140
Submission Type
Review Panel
MI
Medical Specialty
Microbiology
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K801858thoracelOXYMETER & TRANSOXODEAugust 13, 1980