510(k) K981827
K981827 is an FDA 510(k) premarket notification submitted by Angiolaz, Inc. for the device "VES 0281-M COMPLETE VIDEO ENDOSCOPIC VIDEO SYSTEM". The FDA issued a decision of Substantially Equivalent on July 28, 1998. The device falls under product code FET (Endoscopic Video Imaging System/Component, Gastroenterology-Urology), a Class II device regulated under 21 CFR 876.1500. Angiolaz, Inc. has at least 9 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 28, 1998
- Date Received
- May 22, 1998
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Endoscopic Video Imaging System/Component, Gastroenterology-Urology
- Device Class
- Class II
- Regulation Number
- 876.1500
- Review Panel
- GU
- Submission Type
To allow for visualization of body cavities through an endoscope by projecting images to a monitor.