510(k) K921875

X-RAY CONTROL AND HI-VOLTAGE GENERATOR by Continental X-Ray Corp. — Product Code IZO

K921875 is an FDA 510(k) premarket notification submitted by Continental X-Ray Corp. for the device "X-RAY CONTROL AND HI-VOLTAGE GENERATOR". The FDA issued a decision of Substantially Equivalent on October 15, 1992. The device falls under product code IZO (Generator, High-Voltage, X-Ray, Diagnostic), a Class I device regulated under 21 CFR 892.1700. Continental X-Ray Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 15, 1992
Date Received
April 20, 1992
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