JTB — Device, Media Dispensing/Stacking Class I

FDA Device Classification

FDA product code JTB covers "Device, Media Dispensing/Stacking", a Class I medical device regulated under 21 CFR 866.2440. Submissions are reviewed by the Microbiology panel. At least 2 recent 510(k) clearances have been granted under this product code.

Classification Details

Product Code
JTB
Device Class
Class I
Regulation Number
866.2440
Submission Type
Review Panel
MI
Medical Specialty
Microbiology
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K802561acaciaHI VOLUME PUMPING CHAMBEROctober 31, 1980
K790514diagnostic productsI NETILMICIN RIA KITMay 3, 1979