Clearance Summary
PROVIAL II #006-010-0201 received FDA 510(k) clearance under submission number K823773, sponsored by Dynatech Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Pathology review panel. The statutory decision date of record is 1983-01-21.
- Submission: K823773
- Applicant / Sponsor: Dynatech Corp.
- Clearance pathway: Traditional
- Review panel: Pathology
- Device class: Class I
- Regulation citation: 21 CFR 864.3250
- Decision date: 1983-01-21
Classification & Regulation
This clearance is catalogued under FDA product code KDT and 21 CFR 864.3250, within the Pathology review panel as a Class I device.