MFJ — Device, Endoscopic Suturing Class II

FDA Device Classification

FDA product code MFJ covers "Device, Endoscopic Suturing", a Class II medical device regulated under 21 CFR 876.1500. Submissions are reviewed by the Gastroenterology, Urology panel. At least 1 recent 510(k) clearance has been granted under this product code.

Classification Details

Product Code
MFJ
Device Class
Class II
Regulation Number
876.1500
Submission Type
Review Panel
SU
Medical Specialty
Gastroenterology, Urology
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K905722laparomedSUTURE APPLIER DEVICEMarch 14, 1991