Clearance Summary
REP(R) SPE TEMPLATE 30, 16, & 8 received FDA 510(k) clearance under submission number K913807, sponsored by Helena Laboratories. 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 1991-11-27.
- Submission: K913807
- Applicant / Sponsor: Helena Laboratories
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class I
- Regulation citation: 21 CFR 862.1630
- Decision date: 1991-11-27
Classification & Regulation
This clearance is catalogued under FDA product code CEF and 21 CFR 862.1630, within the Clinical Chemistry review panel as a Class I device.