Richard-Allan Medical is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Richard-Allan Medical - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Richard-Allan Medical has 8 FDA 510(k) cleared medical devices. Based in Richland, US.
Historical record: 8 cleared submissions from 1991 to 1994. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Richard-Allan Medical Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Richard-Allan Medical
8 devices
Cleared
May 27, 1994
REFLEX INS INSUFFLATION NEEDLE
Obstetrics & Gynecology
22d
Cleared
Feb 22, 1994
REFLEX ESP WITH FINGER SWITCHES
General & Plastic Surgery
123d
Cleared
Nov 23, 1993
REFLEX SDD SURGICAL STAPLER
General & Plastic Surgery
126d
Cleared
Nov 19, 1993
REFLEX(R) EHS (ENDOSCOPIC HERNIA STAPLER)
General & Plastic Surgery
101d
Cleared
Jul 23, 1993
REFLEX(R) ESP
General & Plastic Surgery
298d
Cleared
Jul 21, 1993
REFLEX(R) ECA
General & Plastic Surgery
294d
Cleared
Feb 19, 1991
RICHARD-ALLAN CLAMP COVERS
General & Plastic Surgery
62d
Cleared
Feb 19, 1991
RICHARD-ALLAN SHEET CLIP
General Hospital
61d