Clearance Summary
CONFLUENT SURGICAL DUAL LIQUID APPLICATOR, MODEL 70-2005093 received FDA 510(k) clearance under submission number K042588, sponsored by Confluent Surgical,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 2004-12-09.
- Submission: K042588
- Applicant / Sponsor: Confluent Surgical,Inc
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class II
- Regulation citation: 21 CFR 880.5860
- Decision date: 2004-12-09
Classification & Regulation
This clearance is catalogued under FDA product code FMF and 21 CFR 880.5860, within the General Hospital review panel as a Class II device.