510(k) K134005
K134005 is an FDA 510(k) premarket notification submitted by Intromedic Co., Ltd. for the device "MIROCAM CAPSULE ENDOSCOPE SYSTEM". The FDA issued a decision of Substantially Equivalent on July 9, 2014. The device falls under product code NEZ (System, Imaging, Gastrointestinal, Wireless, Capsule), a Class II device regulated under 21 CFR 876.1300. Intromedic Co., Ltd. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 9, 2014
- Date Received
- December 27, 2013
- 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