R. J. Doyle, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
R. J. Doyle, Inc. - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
R. J. Doyle, Inc. has 10 FDA 510(k) cleared medical devices. Based in Spokane, US.
Historical record: 10 cleared submissions from 1987 to 1989. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by R. J. Doyle, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - R. J. Doyle, Inc.
10 devices
Cleared
Nov 30, 1989
16GA X 6 BULLET POINT NEEDLE, FLEX STAINLESS STEE
Anesthesiology
121d
Cleared
Nov 30, 1989
16GA X 10 MIDDLE SIZE BULLET POINT NEEDLE
Anesthesiology
121d
Cleared
Nov 30, 1989
16GA X 14 FOURTEEN LONG LONG BULLET POINT NEEDL
Anesthesiology
121d
Cleared
Nov 30, 1989
20GA X 7-1/2 THREADING BULLET POINT NEEDLE
Anesthesiology
121d
Cleared
Nov 30, 1989
INFILTRATION PUMP SYRINGE
Anesthesiology
121d
Cleared
Sep 22, 1989
16 GA X 6 BULLET POINT NEEDLE
General & Plastic Surgery
52d
Cleared
Sep 22, 1989
16 GA X 10 BULLET POINT NEEDLE
General & Plastic Surgery
52d
Cleared
Sep 22, 1989
14 INCH BULLET POINT NEEDLE
General & Plastic Surgery
52d
Cleared
Sep 22, 1989
20GA X 7-1/2 THREADING BULLET POINT NEEDLE
General & Plastic Surgery
52d
Cleared
Jun 25, 1987
HAMACHER BULLET POINT OPHTHALMIC NEEDLE
Ophthalmic
17d