510(k) K132027
K132027 is an FDA 510(k) premarket notification submitted by Ge Oec Medical Systems, Inc. for the device "OEC 9800 PLUS". The FDA issued a decision of Substantially Equivalent on May 1, 2014. The device falls under product code OWB (Interventional Fluoroscopic X-Ray System), a Class II device regulated under 21 CFR 892.1650. Ge Oec Medical Systems, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 1, 2014
- Date Received
- July 1, 2013
- Clearance Type
- Special
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Interventional Fluoroscopic X-Ray System
- Device Class
- Class II
- Regulation Number
- 892.1650
- Review Panel
- RA
- Submission Type
Interventional fluoroscopy