Clearance Summary
MODIFICATION TO AUGUSTINE MEDICAL WOUND CARE SYSTEM, MODEL 68XXX received FDA 510(k) clearance under submission number K020077, sponsored by Augustine Medical, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2002-01-31.
- Submission: K020077
- Applicant / Sponsor: Augustine Medical, Inc.
- Clearance pathway: Special
- Review panel: General, Plastic Surgery
- Device class: Class I
- Regulation citation: 21 CFR 878.4020
- Decision date: 2002-01-31
Classification & Regulation
This clearance is catalogued under FDA product code MSA and 21 CFR 878.4020, within the General, Plastic Surgery review panel as a Class I device.