Clearance Summary
SEDIPLAST received FDA 510(k) clearance under submission number K840500, sponsored by Precision Technology, 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 1984-02-21.
- Submission: K840500
- Applicant / Sponsor: Precision Technology, Inc.
- Clearance pathway: Traditional
- Review panel: Hematology
- Device class: Class I
- Regulation citation: 21 CFR 864.6700
- Decision date: 1984-02-21
Classification & Regulation
This clearance is catalogued under FDA product code JPH and 21 CFR 864.6700, within the Hematology review panel as a Class I device.