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ORTHOLUX VISIBLE LIGHT CURING UNIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K880392
510(k) Type
Traditional
Applicant
UNITEK CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/7/1988
Days to Decision
69 days

ORTHOLUX VISIBLE LIGHT CURING UNIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K880392
510(k) Type
Traditional
Applicant
UNITEK CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/7/1988
Days to Decision
69 days