FLOSS CARD
FDA 510(k) clearance K882164 · decided 1988-06-10
Clearance details
- K-number
- K882164
- Device name
- FLOSS CARD
- Applicant
- Arthur Blank & Co., Inc.
- Decision
- Substantially Equivalent
- Date received
- 1988-05-24
- Decision date
- 1988-06-10
- Days to decision
- 17 days
- Clearance type
- Traditional
- Product code
- JES
- Device class
- 1
- Regulation number
- 872.6390
- Medical specialty
- Dental
- Advisory committee
- Dental
- Location
- Boston, MA, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.