LIEBEL-FLARSHEIM SERIES 8000 BUCKY,W/NON SIZE SENS— 510(k) K903160
Substantially EquivalentContinental X-Ray Corp.
FDA 510(k) clearance K903160 for LIEBEL-FLARSHEIM SERIES 8000 BUCKY,W/NON SIZE SENS, Substantially Equivalent on 1990-08-08. Applicant: Continental X-Ray Corp.. Device class: 2.
Clearance details
- Applicant
- Continental X-Ray Corp.
- Product code
- Code IXQ
- Device class
- Class 2
- Regulation
- 21 CFR 892.1980
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Broadview, IL, US
Recent devices under product code IXQ
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Data sourced from openFDA. This site is unofficial and independent of the FDA.