Clearance Summary
HEPES BUFFER IM IN NORMAL SALINE received FDA 510(k) clearance under submission number K844877, sponsored by Hazleton Research Products, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 1985-02-25.
- Submission: K844877
- Applicant / Sponsor: Hazleton Research Products, Inc.
- Clearance pathway: Traditional
- Review panel: Hematology
- Device class: Class I
- Regulation citation: 21 CFR 864.2875
- Decision date: 1985-02-25
Classification & Regulation
This clearance is catalogued under FDA product code KIP and 21 CFR 864.2875, within the Hematology review panel as a Class I device.