DENTIN PROTECTOR
FDA 510(k) clearance K901915 · decided 1990-06-27
Clearance details
- K-number
- K901915
- Device name
- DENTIN PROTECTOR
- Applicant
- Ivoclar North America, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1990-04-26
- Decision date
- 1990-06-27
- Days to decision
- 62 days
- Clearance type
- Traditional
- Product code
- LBH
- Device class
- 2
- Regulation number
- 872.3260
- Medical specialty
- Dental
- Advisory committee
- Dental
- Location
- Amherst, NY, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.