EZ REGULAR
FDA 510(k) clearance K080303 · decided 2008-08-05
Clearance details
- K-number
- K080303
- Device name
- EZ REGULAR
- Applicant
- Meinntech Co., Ltd.
- Decision
- Substantially Equivalent
- Date received
- 2008-02-05
- Decision date
- 2008-08-05
- Days to decision
- 182 days
- Clearance type
- Traditional
- Product code
- FPA
- Device class
- 2
- Regulation number
- 880.5440
- Medical specialty
- General Hospital
- Advisory committee
- General Hospital
- Location
- Deer Field, IL, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.