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COHERENT SYSTEM 920 ARGON/DYE PHOTOCOAGULATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K882160
510(k) Type
Traditional
Applicant
COHERENT MEDICAL LASERS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/22/1988
Days to Decision
30 days

COHERENT SYSTEM 920 ARGON/DYE PHOTOCOAGULATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K882160
510(k) Type
Traditional
Applicant
COHERENT MEDICAL LASERS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/22/1988
Days to Decision
30 days