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PORTALASE 300 CARBON DIOXIDE SURG LASER EAR/NOSE/T

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K854471
510(k) Type
Traditional
Applicant
MINNESOTA LASER CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/13/1986
Days to Decision
99 days

PORTALASE 300 CARBON DIOXIDE SURG LASER EAR/NOSE/T

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K854471
510(k) Type
Traditional
Applicant
MINNESOTA LASER CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/13/1986
Days to Decision
99 days