JTM — Anaerobic Box Glove Class I

FDA Device Classification

FDA product code JTM covers "Anaerobic Box Glove", a Class I medical device regulated under 21 CFR 866.2120. 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
JTM
Device Class
Class I
Regulation Number
866.2120
Submission Type
Review Panel
MI
Medical Specialty
Microbiology
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K800430oxoid u.s.aOXIDE ANAEROBIC SYSTEMApril 2, 1980