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ULTRAPULSE(TM) CARBON DIOXIDE SURGICAL LASER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K912029
510(k) Type
Traditional
Applicant
COHERENT MEDICAL GROUP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/13/1991
Days to Decision
98 days
Submission Type
Statement

ULTRAPULSE(TM) CARBON DIOXIDE SURGICAL LASER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K912029
510(k) Type
Traditional
Applicant
COHERENT MEDICAL GROUP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/13/1991
Days to Decision
98 days
Submission Type
Statement