MD-FLEX HEAVY BODY
FDA 510(k) clearance K134008 · decided 2014-04-09
Clearance details
- K-number
- K134008
- Device name
- MD-FLEX HEAVY BODY
- Applicant
- Meta Biomed, Inc.
- Decision
- Substantially Equivalent
- Date received
- 2013-12-30
- Decision date
- 2014-04-09
- Days to decision
- 100 days
- Clearance type
- Traditional
- Product code
- ELW
- Device class
- 2
- Regulation number
- 872.3660
- Medical specialty
- Dental
- Advisory committee
- Dental
- Location
- Mt. Airy, MD, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.