Clearance Summary
ZEEMAN 3030 ATOMIC ABSORPT SPECTORPHOT received FDA 510(k) clearance under submission number K842752, sponsored by The Perkin-Elmer Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 1984-08-22.
- Submission: K842752
- Applicant / Sponsor: The Perkin-Elmer Corp.
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class I
- Regulation citation: 21 CFR 862.2850
- Decision date: 1984-08-22
Classification & Regulation
This clearance is catalogued under FDA product code JXR and 21 CFR 862.2850, within the Clinical Chemistry review panel as a Class I device.