SUPER FLOSSER
FDA 510(k) clearance K874471 · decided 1988-01-28
Clearance details
- K-number
- K874471
- Device name
- SUPER FLOSSER
- Applicant
- U.S. Pacific Corp.
- Decision
- Substantially Equivalent
- Date received
- 1987-11-02
- Decision date
- 1988-01-28
- Days to decision
- 87 days
- Clearance type
- Traditional
- Product code
- JES
- Device class
- 1
- Regulation number
- 872.6390
- Medical specialty
- Dental
- Advisory committee
- Dental
- Location
- Bloomfield Hills, MI, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.