510(k) K031771
K031771 is an FDA 510(k) premarket notification submitted by Shimadzu Corp. for the device "SHIMADZU COLLIMATOR R-30H". The FDA issued a decision of Substantially Equivalent on August 21, 2003. The device falls under product code IZX (Collimator, Manual, Radiographic), a Class II device regulated under 21 CFR 892.1610. Shimadzu Corp. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 21, 2003
- Date Received
- June 9, 2003
- Clearance Type
- Abbreviated
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Collimator, Manual, Radiographic
- Device Class
- Class II
- Regulation Number
- 892.1610
- Review Panel
- RA
- Submission Type