Byron Medical is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Byron Medical - FDA 510(k) Cleared Devices
Recent clearances: PSI-TEC PERISTALTIC INFILTRATION PUMP, ACCELERATOR RECIPROCATING CANNULA, PSI-TEC LIPOSUCTION ASPIRATOR
27
Total
24
Cleared
0
Denied
Byron Medical has 24 FDA 510(k) cleared general & plastic surgery devices. Based in Tucson, US.
Historical record: 24 cleared submissions from 1986 to 2004.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Byron Medical
27 devices
Cleared
Jun 03, 2004
PSI-TEC PERISTALTIC INFILTRATION PUMP
General Hospital
132d
Cleared
Aug 04, 2000
ACCELERATOR RECIPROCATING CANNULA
General & Plastic Surgery
51d
Cleared
Jul 01, 1998
PSI-TEC LIPOSUCTION ASPIRATOR
General & Plastic Surgery
90d
Cleared
Jun 30, 1998
LIPOPLASTY/ LIPOSUCTION ASPIRATION AND TUMESCENT INFUSION CANNULAE AND NEEDLES
General & Plastic Surgery
90d
Cleared
Jun 16, 1998
PSI-TEC SYRINGE INFUSION PUMP AND ACCESSORIES FOR GENERAL FLUID...
General Hospital
111d
Cleared
Mar 05, 1998
PSI-TEC ASPIRATOR
General & Plastic Surgery
31d
Cleared
Feb 10, 1998
BYRON MEDICAL ASPIRATION AND INFILTRATION/IRRIGATION TUBING
General & Plastic Surgery
88d
Cleared
Sep 12, 1997
BIG BAG 3000 PRESSURE INFUSOR
General Hospital
22d
Cleared
May 23, 1994
DISPOSABLE BAG DECANTER
General Hospital
270d
Cleared
Feb 03, 1994
ZARA ZONE IV MALAR IMPLANT MODIFICATION
General & Plastic Surgery
157d
Cleared
Jan 07, 1994
BIOPSY PUNCH, SURGICAL
Dental
163d
Cleared
Apr 21, 1992
ZARA SILICONE BLOCK
General & Plastic Surgery
236d