Clearance Summary
KIT, PREP, INSPIRON IV received FDA 510(k) clearance under submission number K760313, sponsored by Inspiron Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 1976-08-04.
- Submission: K760313
- Applicant / Sponsor: Inspiron Corp.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class I
- Regulation citation: 21 CFR 880.5420
- Decision date: 1976-08-04
Classification & Regulation
This clearance is catalogued under FDA product code KZD and 21 CFR 880.5420, within the General Hospital review panel as a Class I device.