KIN — Slide Stainer, Contact Type Class I

FDA Device Classification

FDA product code KIN covers "Slide Stainer, Contact Type", a Class I medical device regulated under 21 CFR 864.3800. 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
KIN
Device Class
Class I
Regulation Number
864.3800
Submission Type
Review Panel
PA
Medical Specialty
Pathology
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K760032gamma biologicalsTEST, MONO., DIFFERENTIAL SLIDEAugust 3, 1976