Clearance Summary
AIDA COMPACT II SYSTEM received FDA 510(k) clearance under submission number K052159, sponsored by KARL STORZ Endoscopy-America, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2005-09-07.
- Submission: K052159
- Applicant / Sponsor: KARL STORZ Endoscopy-America, Inc.
- Clearance pathway: Special
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.2050
- Decision date: 2005-09-07
Classification & Regulation
This clearance is catalogued under FDA product code LLZ and 21 CFR 892.2050, within the Radiology review panel as a Class II device.