Last synced on 14 November 2025 at 11:06 pm

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

Page Type
Cleared 510(K)
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)
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