Clearance Summary
HEMOGLOBINOMETER MODEL 720 B received FDA 510(k) clearance under submission number K781361, sponsored by Innovative Medical Systems, 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 1978-09-14.
- Submission: K781361
- Applicant / Sponsor: Innovative Medical Systems, Inc.
- Clearance pathway: Traditional
- Review panel: Hematology
- Device class: Class II
- Regulation citation: 21 CFR 864.5620
- Decision date: 1978-09-14
Classification & Regulation
This clearance is catalogued under FDA product code GKR and 21 CFR 864.5620, within the Hematology review panel as a Class II device.