510(k) K827609
K827609 is an FDA 510(k) premarket notification submitted by Midwest X-Ray Equipment Co. for the device "MIDWEST AUTOMATIC BUCKY EQUIPPED WITH GRID AND SIZE-O-MATIC TRAY". The FDA issued a decision of Substantially Equivalent on July 9, 1982. Midwest X-Ray Equipment Co. has at least 2 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 9, 1982
- Date Received
- June 8, 1982
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No