510(k) K896119
K896119 is an FDA 510(k) premarket notification submitted by Rms Div. for the device "RMS 90/15 RADIOGRAPHIC/FLUOROSCOPIC TILTING TABLE". The FDA issued a decision of Substantially Equivalent on November 27, 1989. The device falls under product code IXR (Table, Radiographic, Tilting), a Class II device regulated under 21 CFR 892.1980. Rms Div. has at least 9 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- November 27, 1989
- Date Received
- October 24, 1989
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Table, Radiographic, Tilting
- Device Class
- Class II
- Regulation Number
- 892.1980
- Review Panel
- RA
- Submission Type