Clearance Summary
BLUESKY VISTA WOUND VACUUM SYSTEM, MODEL 100.0500 received FDA 510(k) clearance under submission number K061367, sponsored by Blue Sky Medical Group Incorporated. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2006-08-10.
- Submission: K061367
- Applicant / Sponsor: Blue Sky Medical Group Incorporated
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.4780
- Decision date: 2006-08-10
Classification & Regulation
This clearance is catalogued under FDA product code OMP and 21 CFR 878.4780, within the General, Plastic Surgery review panel as a Class II device.