KSD — Device, Heat-Sealing Class I

FDA Device Classification

FDA product code KSD covers "Device, Heat-Sealing", a Class I medical device regulated under 21 CFR 864.9750. Submissions are reviewed by the Hematology panel. At least 1 recent 510(k) clearance has been granted under this product code.

Classification Details

Product Code
KSD
Device Class
Class I
Regulation Number
864.9750
Submission Type
Review Panel
HE
Medical Specialty
Hematology
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K820301north american biologicalsPLASMA POOLER HEAT SEALERApril 9, 1982