510(k) K902606
K902606 is an FDA 510(k) premarket notification submitted by Professional Medical Services for the device "RADIOPAQUE RULER". The FDA issued a decision of Substantially Equivalent on September 27, 1990. The device falls under product code KPR (System, X-Ray, Stationary), a Class II device regulated under 21 CFR 892.1680. Professional Medical Services has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- September 27, 1990
- Date Received
- June 12, 1990
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- System, X-Ray, Stationary
- Device Class
- Class II
- Regulation Number
- 892.1680
- Review Panel
- RA
- Submission Type