GE 900— 510(k) K811103
Substantially EquivalentGeneral Electric Co.
FDA 510(k) clearance K811103 for GE 900, Substantially Equivalent on 1981-06-09. Applicant: General Electric Co.. Device class: 2.
Clearance details
- Applicant
- General Electric Co.
- Product code
- Code EHD
- Device class
- Class 2
- Regulation
- 21 CFR 872.1800
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
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