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MODEL 920 ARGON/DYE LASER-FOR DERMATOLOGICAL/USE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K852860
510(k) Type
Traditional
Applicant
COHERENT MEDICAL GROUP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/7/1985
Days to Decision
91 days

MODEL 920 ARGON/DYE LASER-FOR DERMATOLOGICAL/USE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K852860
510(k) Type
Traditional
Applicant
COHERENT MEDICAL GROUP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/7/1985
Days to Decision
91 days