Clearance Summary
TISSUE CULTURE TUBES received FDA 510(k) clearance under submission number K873889, sponsored by Nunc, 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 1987-11-25.
- Submission: K873889
- Applicant / Sponsor: Nunc, Inc.
- Clearance pathway: Traditional
- Review panel: Hematology
- Device class: Class I
- Regulation citation: 21 CFR 864.2240
- Decision date: 1987-11-25
Classification & Regulation
This clearance is catalogued under FDA product code KJA and 21 CFR 864.2240, within the Hematology review panel as a Class I device.