Gettig Pharmaceutical Instrument Co. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Gettig Pharmaceutical Instrument Co. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Gettig Pharmaceutical Instrument Co. has 5 FDA 510(k) cleared medical devices. Based in Great Neck, US.
Historical record: 5 cleared submissions from 1997 to 2004. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Gettig Pharmaceutical Instrument Co. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Gettig Pharmaceutical Instrument Co.
5 devices
Cleared
Jul 22, 2004
GETTIG UNIVERSAL VIAL ACCESS PIN
General Hospital
73d
Cleared
Jan 21, 2004
AMERSHAM HEALTH NEEDLE-GUARD
General Hospital
89d
Cleared
Oct 08, 2002
GETTIG DISPOSABLE SYRINGES
General Hospital
71d
Cleared
Apr 19, 2000
GETTIG GUARD
General Hospital
68d
Cleared
Sep 11, 1997
GETTIG STYRL-JECT DELIVERY SYSTEM
Dental
84d