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MODEL ML-820 CARBON DIOXIDE LASER SYSTEM FOR SURGERY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K827506
510(k) Type
Traditional
Applicant
MERRIMACK LABORATORIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/11/1982
Days to Decision
38 days

MODEL ML-820 CARBON DIOXIDE LASER SYSTEM FOR SURGERY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K827506
510(k) Type
Traditional
Applicant
MERRIMACK LABORATORIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/11/1982
Days to Decision
38 days