Clearance Summary
STRYKER ECLIPSE WARMING STRETCHER received FDA 510(k) clearance under submission number K912237, sponsored by Stryker Medical. 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 1991-07-30.
- Submission: K912237
- Applicant / Sponsor: Stryker Medical
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class I
- Regulation citation: 21 CFR 878.4820
- Decision date: 1991-07-30
Classification & Regulation
This clearance is catalogued under FDA product code DWI and 21 CFR 878.4820, within the General, Plastic Surgery review panel as a Class I device.