FDA · official record K020062Substantially EquivalentXERAFIT
United StatesEJHMetalor Technologies USA
Official record identity
- FDA application number
- K020062
- Decision date
- February 14, 2002
- Published decision
- Substantially Equivalent
Classification
Published parties
- Applicant
- Metalor Technologies USA
Additional source fields
- Decision code
- SESE
- Published decision
- Substantially Equivalent
- Submission type
- Traditional
- Received date
- 2002-01-08
- Review panel
- Dental
- Current product-code class (harmonized)
- 2
- Current product-code regulation (harmonized)
- 872.3710
About this record
This record preserves an application published in the FDA 510(k) bulk export, including the DEN entries FDA includes in that export. Historical decisions do not establish current marketing status. Product-code harmonization is separate from the original application; joined establishment identifiers are not assigned to the applicant. The complete official export is checked daily and raw evidence is retained.