9170, 1170— 510(k) K932354
Substantially EquivalentDynarad Corp.
FDA 510(k) clearance K932354 for 9170, 1170, Substantially Equivalent on 1993-07-23. Applicant: Dynarad Corp.. Device class: 2.
Clearance details
- Applicant
- Dynarad Corp.
- Product code
- Code IZL
- Device class
- Class 2
- Regulation
- 21 CFR 892.1720
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Deer Park, NY, US
Recent devices under product code IZL
view allMore clearances from Dynarad Corp.
view allAdverse events under product code IZL
product code IZL- Other
- 3
- Total
- 3
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.