Clearance Summary
TARGET READER received FDA 510(k) clearance under submission number K885254, sponsored by V-Tech, Inc.. 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 1989-01-27.
- Submission: K885254
- Applicant / Sponsor: V-Tech, Inc.
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class I
- Regulation citation: 21 CFR 862.2400
- Decision date: 1989-01-27
Classification & Regulation
This clearance is catalogued under FDA product code JQT and 21 CFR 862.2400, within the Clinical Chemistry review panel as a Class I device.