Clearance Summary
CARAWAY TUBES, HEPARIN AND PLAIN received FDA 510(k) clearance under submission number K881262, sponsored by Helps 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 1988-05-06.
- Submission: K881262
- Applicant / Sponsor: Helps Products, Inc.
- Clearance pathway: Traditional
- Review panel: Hematology
- Device class: Class I
- Regulation citation: 21 CFR 864.6150
- Decision date: 1988-05-06
Classification & Regulation
This clearance is catalogued under FDA product code GIO and 21 CFR 864.6150, within the Hematology review panel as a Class I device.