GDL — Needle, Suturing, Reusable Class I

FDA Device Classification

Classification Details

Product Code
GDL
Device Class
Class I
Regulation Number
878.4800
Submission Type
Review Panel
SU
Medical Specialty
General, Plastic Surgery
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K881394china national medicines c/o havelNON-STERILE SUTURE NEEDLESApril 8, 1988
K851781artiberia25-420 TO 25-436 VARIOUS TYPES OF SUTURE NEEDLESJune 20, 1985
K851782artiberia25-450 TO 25-540 VARIOUS SUTURE FORCEPSJune 20, 1985
K813589s. jacksonSHARTPOINT EYED NEEDLESJanuary 18, 1982
K812566ortho pared instrumentsUNIVERSAL SUTURE PASSERNovember 10, 1981