510(k) K163069
K163069 is an FDA 510(k) premarket notification submitted by Olympus Medical Systems Corp. for the device "OLYMPUS SMALL INTESTINAL CAPSULE ENDOSCOPE SYSTEM". The FDA issued a decision of Substantially Equivalent on January 19, 2017. The device falls under product code NEZ (System, Imaging, Gastrointestinal, Wireless, Capsule), a Class II device regulated under 21 CFR 876.1300. Olympus Medical Systems Corp. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 19, 2017
- Date Received
- November 2, 2016
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- System, Imaging, Gastrointestinal, Wireless, Capsule
- Device Class
- Class II
- Regulation Number
- 876.1300
- Review Panel
- GU
- Submission Type