Clearance Summary
PERKINELMER 226 SAMPLE COLLECTION DEVICES received FDA 510(k) clearance under submission number K121864, sponsored by Perkinelmer, Inc.. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 2013-03-12.
- Submission: K121864
- Applicant / Sponsor: Perkinelmer, Inc.
- Clearance pathway: Abbreviated
- Review panel: Clinical Chemistry
- Device class: Class II
- Regulation citation: 21 CFR 862.1675
- Decision date: 2013-03-12
Classification & Regulation
This clearance is catalogued under FDA product code PJC and 21 CFR 862.1675, within the Clinical Chemistry review panel as a Class II device.