Clearance Summary
TRI-TECH INC. CUSTOM SEXUAL ASSAULT KIT received FDA 510(k) clearance under submission number K922343, sponsored by Tri-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 1994-02-17.
- Submission: K922343
- Applicant / Sponsor: Tri-Tech, Inc.
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class II
- Regulation citation: 21 CFR 862.1675
- Decision date: 1994-02-17
Classification & Regulation
This clearance is catalogued under FDA product code JKA and 21 CFR 862.1675, within the Clinical Chemistry review panel as a Class II device.