Clearance Summary
INSPECTRA TISSUE SPECTROMETER SYSTEM (INSPECTRA), MODEL 325 received FDA 510(k) clearance under submission number K012759, sponsored by Hutchinson Technology, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2002-01-17.
- Submission: K012759
- Applicant / Sponsor: Hutchinson Technology, Inc.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.2700
- Decision date: 2002-01-17
Classification & Regulation
This clearance is catalogued under FDA product code MUD and 21 CFR 870.2700, within the Cardiovascular review panel as a Class II device.