Gettig Pharmaceutical Instrument Co.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 5
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K041232 | GETTIG UNIVERSAL VIAL ACCESS PIN | July 22, 2004 |
| K033409 | AMERSHAM HEALTH NEEDLE-GUARD | January 21, 2004 |
| K022495 | GETTIG DISPOSABLE SYRINGES | October 8, 2002 |
| K000455 | GETTIG GUARD | April 19, 2000 |
| K972285 | GETTIG STYRL-JECT DELIVERY SYSTEM | September 11, 1997 |