HELIOS LASER IMAGER 1417— 510(k) K973028
Substantially EquivalentSterling Diagnostic Imaging, Inc.
FDA 510(k) clearance K973028 for HELIOS LASER IMAGER 1417, Substantially Equivalent on 1997-10-28. Applicant: Sterling Diagnostic Imaging, Inc.. Device class: 2.
Clearance details
- Applicant
- Sterling Diagnostic Imaging, Inc.
- Product code
- Code LMC
- Device class
- Class 2
- Regulation
- 21 CFR 892.2040
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Greenville, SC, US
Recent devices under product code LMC
view allMore clearances from Sterling Diagnostic Imaging, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.