510(k) K921425
K921425 is an FDA 510(k) premarket notification submitted by Acoma Medical Imaging, Inc. for the device "SCD-105 AND SCD-125 CAPACITOR DISCHARGE MOBILE X-R". The FDA issued a decision of Substantially Equivalent on August 27, 1992. The device falls under product code IZL (System, X-Ray, Mobile), a Class II device regulated under 21 CFR 892.1720. Acoma Medical Imaging, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 27, 1992
- Date Received
- March 24, 1992
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- System, X-Ray, Mobile
- Device Class
- Class II
- Regulation Number
- 892.1720
- Review Panel
- RA
- Submission Type