Phoenix Medical Technology, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Phoenix Medical Technology, Inc. - FDA 510(k) Cleared Devices
11
Total
11
Cleared
0
Denied
Phoenix Medical Technology, Inc. has 11 FDA 510(k) cleared general hospital devices. Based in Andrews, US.
Historical record: 11 cleared submissions from 1986 to 2000.
Browse the complete list of FDA 510(k) cleared general hospital devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Phoenix Medical Technology, Inc.
11 devices
Cleared
Apr 14, 2000
NITRILE PATIENT EXAMINATION GLOVES, POWDER-FREE
General Hospital
81d
Cleared
Jan 02, 1995
PATIENT EXAINATION GLOVES
General Hospital
80d
Cleared
Jan 18, 1991
PATIENT EXAMINATION GLOVES
General Hospital
72d
Cleared
Feb 13, 1990
MODIFIED SINGLE USE LATEX EXAMINATION GLOVES
General Hospital
14d
Cleared
Feb 13, 1990
MODIFIED LOW POWDER SINGLE USE LATEX EXAM GLOVES
General Hospital
14d
Cleared
Aug 17, 1989
PHOENIX DRAPES WITH MICROBAN
General & Plastic Surgery
175d
Cleared
Jun 22, 1989
SINGLE USE VINYL EXAM GLOVES - COLOR CODED
General Hospital
71d
Cleared
Jun 19, 1989
LOW POWDER SINGLE USE LATEX EXAM GLOVES
General Hospital
68d
Cleared
May 25, 1989
PATIENT EXAMINATION GLOVES (LATEX)
General Hospital
58d
Cleared
Mar 22, 1989
PATIENT EXAMINATION GLOVE
General Hospital
19d
Cleared
Feb 28, 1986
DOBE (MODIFIED)
Cardiovascular
154d