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BIOPTRON PRO LIGHT THERAPY SYSTEM AND BIOPTRON COMPACT III LIGHT THERAPY SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032216
510(k) Type
Traditional
Applicant
Bioptron AG
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/4/2004
Days to Decision
198 days
Submission Type
Statement

BIOPTRON PRO LIGHT THERAPY SYSTEM AND BIOPTRON COMPACT III LIGHT THERAPY SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032216
510(k) Type
Traditional
Applicant
Bioptron AG
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/4/2004
Days to Decision
198 days
Submission Type
Statement