Richard Hamer Assoc., Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Richard Hamer Assoc., Inc. - FDA 510(k) Cleared Devices
8
Total
6
Cleared
0
Denied
Richard Hamer Assoc., Inc. has 6 FDA 510(k) cleared medical devices. Based in Fort Worth, US.
Historical record: 6 cleared submissions from 1993 to 1996. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Richard Hamer Assoc., Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Richard Hamer Assoc., Inc.
8 devices
Cleared
Sep 03, 1996
DERMAPLEX HYDROGEL WOUND DRESSING (2X2,4X4,4X8,6X10)
General & Plastic Surgery
71d
Cleared
Jul 31, 1995
COMFEEL PLUS PRESSURE RELIEF DRESSING
General Hospital
130d
Cleared
May 16, 1995
MPM HYDROGEL DRESSING
General & Plastic Surgery
76d
Cleared
Apr 28, 1995
COMFEEL PLUS CONTOUR DRESSING
General & Plastic Surgery
36d
Cleared
Jul 29, 1994
COMFEEL PLUS TRANSPARENT DRESSING
General & Plastic Surgery
79d
Cleared
Jul 18, 1994
COSTELLO-EVERETT LASER CYSTOSCOPE SHEATH
Gastroenterology & Urology
48d
Cleared
May 10, 1994
COMFEEL PLUS WOUND DRESSING
General & Plastic Surgery
55d
Cleared
Dec 22, 1993
MESALT STERILE DRESSING
General & Plastic Surgery
75d