510(k) K901679
K901679 is an FDA 510(k) premarket notification submitted by I.S.G. Technologies, Inc. for the device "RESUBMITTED ISG 3DMV WORKSTATION". The FDA issued a decision of Substantially Equivalent on May 29, 1990. The device falls under product code LLZ (System, Image Processing, Radiological), a Class II device regulated under 21 CFR 892.2050. I.S.G. Technologies, Inc. has at least 9 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 29, 1990
- Date Received
- April 12, 1990
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- System, Image Processing, Radiological
- Device Class
- Class II
- Regulation Number
- 892.2050
- Review Panel
- RA
- Submission Type