Ziehm International, Inc. - FDA 510(k) Cleared Devices
16
Total
16
Cleared
0
Denied
Ziehm International, Inc. has 16 FDA 510(k) cleared medical devices. Based in Annapolis, US.
Historical record: 16 cleared submissions from 1982 to 2001. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Ziehm International, Inc. Filter by specialty or product code using the sidebar.
16 devices
Cleared
Jun 20, 2001
ZIEHM VISION
Radiology
51d
Cleared
Feb 14, 1991
IMS DISPOSABLE HOLDER WITH NEEDLE RETRACTOR
General Hospital
13d
Cleared
Jun 26, 1990
MODIFIED STICK-GARD SAFETY NEEDLE
General Hospital
41d
Cleared
Sep 01, 1989
MOBILE X-RAY UNIT
Radiology
87d
Cleared
Aug 28, 1989
PUMP-JECT SYRINGE WITH LUER-LOCK
General Hospital
83d
Cleared
Feb 28, 1989
STICK-GARD SAFETY NEEDLE
General Hospital
21d
Cleared
Sep 19, 1988
MAMMO M
Radiology
122d
Cleared
Mar 13, 1985
IV ADMIN. SET FOR MVP 1 INFUSION PUMP
General Hospital
202d
Cleared
Jul 25, 1984
MTP E.V. INFUSION PUMP
General Hospital
48d
Cleared
Oct 14, 1983
CARDIAC OUTPUT COMPUTER
Cardiovascular
165d
Cleared
Apr 30, 1983
IV ADMINISTRATION SETS - MVP INFUSION
General Hospital
74d
Cleared
Mar 31, 1983
IMS MINIATURE VOLUMETRIC INFUSION PUMP
General Hospital
44d
Cleared
Oct 15, 1982
BIPOLAR TEMP. PACING CATHETER W/STYLETET
Cardiovascular
99d
Cleared
Oct 15, 1982
BALLOON TEMP. PACING CATHETER
Cardiovascular
99d
Cleared
Aug 24, 1982
BERMAN ANGIOGRAPHIC BALLOON CATHETER
Cardiovascular
43d
Cleared
Aug 24, 1982
BALLOON WEDGE PRESSURE CATHETER
Cardiovascular
43d