510(k) K893652
K893652 is an FDA 510(k) premarket notification submitted by Fischer Imaging Corp. for the device "RADIOGRAPHIC FLOOR MOUNTED TUBESTAND FM 60". The FDA issued a decision of Substantially Equivalent on June 23, 1989. The device falls under product code IYB (Tube Mount, X-Ray, Diagnostic), a Class I device regulated under 21 CFR 892.1770. Fischer Imaging Corp. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 23, 1989
- Date Received
- May 15, 1989
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Tube Mount, X-Ray, Diagnostic
- Device Class
- Class I
- Regulation Number
- 892.1770
- Review Panel
- RA
- Submission Type