Clearance Summary
DR. GOULD HAND PACK SUSTOM STERIL received FDA 510(k) clearance under submission number K842405, sponsored by Pro-Lab, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 1984-08-15.
- Submission: K842405
- Applicant / Sponsor: Pro-Lab, Inc.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class II
- Regulation citation: 21 CFR 880.6850
- Decision date: 1984-08-15
Classification & Regulation
This clearance is catalogued under FDA product code FRG and 21 CFR 880.6850, within the General Hospital review panel as a Class II device.