Clearance Summary
STORZ DIAGNOSTIC MICROSCOPE SYSTEM received FDA 510(k) clearance under submission number K882269, sponsored by Storz Instrument Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 1988-06-23.
- Submission: K882269
- Applicant / Sponsor: Storz Instrument Co.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class I
- Regulation citation: 21 CFR 878.4700
- Decision date: 1988-06-23
Classification & Regulation
This clearance is catalogued under FDA product code EPT and 21 CFR 878.4700, within the General, Plastic Surgery review panel as a Class I device.