Clearance Summary
GLOVE CHECK PATIENT EXAMINATION GLOVE LEAK DETECT. received FDA 510(k) clearance under submission number K915636, sponsored by Associated Ent., 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 1992-07-13.
- Submission: K915636
- Applicant / Sponsor: Associated Ent., Inc.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class:
- Decision date: 1992-07-13
Classification & Regulation
This clearance is catalogued under FDA product code LDQ , within the General Hospital review panel as a device.