Clearance Summary
PNEUMOTHORAX KIT, MODIFICATION received FDA 510(k) clearance under submission number K904021, sponsored by Arrow Intl., Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 1990-10-09.
- Submission: K904021
- Applicant / Sponsor: Arrow Intl., Inc.
- Clearance pathway: Traditional
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3150
- Decision date: 1990-10-09
Classification & Regulation
This clearance is catalogued under FDA product code JDC and 21 CFR 888.3150, within the Orthopedic review panel as a Class II device.