THORAX FD AND MULTIX FD— 510(k) K983732
Substantially EquivalentSiemens Medical Solutions USA, Inc.
FDA 510(k) clearance K983732 for THORAX FD AND MULTIX FD, Substantially Equivalent on 1999-04-21. Applicant: Siemens Medical Solutions USA, Inc.. Device class: 2.
Clearance details
- Applicant
- Siemens Medical Solutions USA, Inc.
- Product code
- Code MQB
- Device class
- Class 2
- Regulation
- 21 CFR 892.1680
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Iselin, NJ, US
Recent devices under product code MQB
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view allRecalls naming K983732
K-number listed on FDA's recall recordMatched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K983732.
Data sourced from openFDA. This site is unofficial and independent of the FDA.