MGI — Aspirator, Ultrasonic Class III

FDA Device Classification

FDA product code MGI covers "Aspirator, Ultrasonic", a Class III medical device. Submissions are reviewed by the Unknown panel. At least 1 recent 510(k) clearance has been granted under this product code.

Classification Details

Product Code
MGI
Device Class
Class III
Regulation Number
Submission Type
Review Panel
OB
Medical Specialty
Unknown
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K913848sharplan lasersSHARPLAN MODEL ULTRA ULTRASONIC SURG ASPIRATORMarch 27, 1992