Clearance Summary
HEMOGLOBIN SCREENING DEVICE received FDA 510(k) clearance under submission number K882101, sponsored by Portable Medical Laboratories, 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 1988-07-01.
- Submission: K882101
- Applicant / Sponsor: Portable Medical Laboratories, Inc.
- Clearance pathway: Traditional
- Review panel: Hematology
- Device class: Class I
- Regulation citation: 21 CFR 864.9320
- Decision date: 1988-07-01
Classification & Regulation
This clearance is catalogued under FDA product code KSL and 21 CFR 864.9320, within the Hematology review panel as a Class I device.