510(k) K920725
K920725 is an FDA 510(k) premarket notification submitted by Shimadzu Medical Systems for the device "COLLIMATOR F-20". The FDA issued a decision of Substantially Equivalent on April 16, 1992. The device falls under product code IZW (Collimator, Automatic, Radiographic), a Class II device regulated under 21 CFR 892.1610. Shimadzu Medical Systems has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- April 16, 1992
- Date Received
- February 18, 1992
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Collimator, Automatic, Radiographic
- Device Class
- Class II
- Regulation Number
- 892.1610
- Review Panel
- RA
- Submission Type