EMD — Hemostat, Surgical Class I

FDA Device Classification

FDA product code EMD covers "Hemostat, Surgical", a Class I medical device regulated under 21 CFR 872.4565. Submissions are reviewed by the Dental panel. At least 2 recent 510(k) clearances have been granted under this product code.

Classification Details

Product Code
EMD
Device Class
Class I
Regulation Number
872.4565
Submission Type
Review Panel
DE
Medical Specialty
Dental
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K920883s.t.s instrumentsHEMOSTAT, SURGICAL (VARIOUS TYPES)March 13, 1992
K770158deringer-neyHEMOSTATJanuary 31, 1977