KIM — Device For Sealing Microsections Class I

FDA Device Classification

FDA product code KIM covers "Device For Sealing Microsections", a Class I medical device regulated under 21 CFR 864.3400. Submissions are reviewed by the Pathology panel. At least 1 recent 510(k) clearance has been granted under this product code.

Classification Details

Product Code
KIM
Device Class
Class I
Regulation Number
864.3400
Submission Type
Review Panel
PA
Medical Specialty
Pathology
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K780261shandonCOVERSLIPPERApril 18, 1978