Clearance Summary
16 X 125 MM TEST TUBE, CATALOG #01-401 received FDA 510(k) clearance under submission number K930386, sponsored by Proteins Intl., 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 1993-03-23.
- Submission: K930386
- Applicant / Sponsor: Proteins Intl., Inc.
- Clearance pathway: Traditional
- Review panel: Hematology
- Device class: Class I
- Regulation citation: 21 CFR 864.2280
- Decision date: 1993-03-23
Classification & Regulation
This clearance is catalogued under FDA product code KIR and 21 CFR 864.2280, within the Hematology review panel as a Class I device.