Clearance Summary
GETTIG STYRL-JECT DELIVERY SYSTEM received FDA 510(k) clearance under submission number K972285, sponsored by Gettig Pharmaceutical Instrument Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1997-09-11.
- Submission: K972285
- Applicant / Sponsor: Gettig Pharmaceutical Instrument Co.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.6770
- Decision date: 1997-09-11
Classification & Regulation
This clearance is catalogued under FDA product code EJI and 21 CFR 872.6770, within the Dental review panel as a Class II device.