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ACULUX, MODEL AX3001, AX3002

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K001223
510(k) Type
Traditional
Applicant
ACULUX
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/23/2000
Days to Decision
67 days
Submission Type
Statement

ACULUX, MODEL AX3001, AX3002

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K001223
510(k) Type
Traditional
Applicant
ACULUX
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/23/2000
Days to Decision
67 days
Submission Type
Statement