Clearance Summary
KELLER PULSE OXIMETER, MODEL 850+ received FDA 510(k) clearance under submission number K982331, sponsored by Keller Medical Specialties Products, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1998-09-11.
- Submission: K982331
- Applicant / Sponsor: Keller Medical Specialties Products, Inc.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.2700
- Decision date: 1998-09-11
Classification & Regulation
This clearance is catalogued under FDA product code DQA and 21 CFR 870.2700, within the Cardiovascular review panel as a Class II device.