DIGITAL X-RAY IMAGING SYSTEM— 510(k) K111103
Substantially EquivalentRf Co., Ltd.
FDA 510(k) clearance K111103 for DIGITAL X-RAY IMAGING SYSTEM, Substantially Equivalent on 2012-01-05. Applicant: Rf Co., Ltd.. Device class: 2.
Clearance details
- Applicant
- Rf Co., Ltd.
- Product code
- Code MUH
- Device class
- Class 2
- Regulation
- 21 CFR 872.1800
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Bunkyo-Ku, Tokyo, JP
Recent devices under product code MUH
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