510(k) K905855
K905855 is an FDA 510(k) premarket notification submitted by Varian Canada, Inc. for the device "VPW2877E7 X RAY POWER SUPPLY". The FDA issued a decision of Substantially Equivalent on February 13, 1991. The device falls under product code IZO (Generator, High-Voltage, X-Ray, Diagnostic), a Class I device regulated under 21 CFR 892.1700. Varian Canada, Inc. has at least 6 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- February 13, 1991
- Date Received
- December 21, 1990
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Generator, High-Voltage, X-Ray, Diagnostic
- Device Class
- Class I
- Regulation Number
- 892.1700
- Review Panel
- RA
- Submission Type