510(k) K941017
K941017 is an FDA 510(k) premarket notification submitted by Acoma Medical Imaging, Inc. for the device "F/C/W TUBESTAND". The FDA issued a decision of Substantially Equivalent on July 29, 1994. The device falls under product code IYB (Tube Mount, X-Ray, Diagnostic), a Class I device regulated under 21 CFR 892.1770. Acoma Medical Imaging, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 29, 1994
- Date Received
- March 3, 1994
- 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