Clearance Summary
NON-STERILE PATIENT EXAMINATION GLOVES received FDA 510(k) clearance under submission number K892772, sponsored by Care-Pro Industries, 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 1989-08-04.
- Submission: K892772
- Applicant / Sponsor: Care-Pro Industries, Inc.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class I
- Regulation citation: 21 CFR 880.6250
- Decision date: 1989-08-04
Classification & Regulation
This clearance is catalogued under FDA product code LYY and 21 CFR 880.6250, within the General Hospital review panel as a Class I device.