S. Jackson, Inc.

16 FDA 510(k) medical device clearances.

Top product codes for S. Jackson, Inc.

FTM — General, Plastic Surgery 6 devices
GAR — General, Plastic Surgery 4 devices
GAW — General, Plastic Surgery 2 devices
FNG — General Hospital 1 device
FTL — General, Plastic Surgery 1 device
FWP — General, Plastic Surgery 1 device
GDL — General, Plastic Surgery 1 device

Recent clearances by S. Jackson, Inc.

K080216 — SUPRAMESH EXTRA FTL · 2008-09-15
K973379 — STERILE SUPRAFOIL SMOOTH NYLON FOIL SHEETS FTM · 1997-09-25
K931612 — NYLAMID SUTURE GAR · 1993-12-17
K931613 — SUPRAMID SUTURE GAR · 1993-12-17
K931614 — MOPYLEN SUTURE GAW · 1993-12-17
K922630 — MOPYLEN GAW · 1992-10-20
K912429 — N80-838 SUPRAMID EXTRA SUTURE GAR · 1991-10-02
K904052 — SUPRAMID EXTRA SUTURES GAR · 1990-10-25
K852011 — NYLAMID MESH PAD FULL & HALF FTM · 1985-06-11
K831725 — FOIL IN 3 FORMS-NON-STERILE SHEETS FTM · 1983-08-16
K831723 — SUPRAMID EXTRA SURGICAL MESH FTM · 1983-08-12
K831724 — CHIN (MENTOPLASTY) IMPLANTS FWP · 1983-08-12
K831727 — QUARTER GLOBE CAPS FTM · 1983-08-12
K831726 — EYE MUSCLE SLEEVES FTM · 1983-08-11
K813589 — SHARTPOINT EYED NEEDLES GDL · 1982-01-18
K802780 — JACKSON HYDRO SYSTEM FNG · 1980-12-10

Data sourced from openFDA. This site is unofficial and independent of the FDA.