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PORTALASE 300 CARBON DIOXIDE SURG LASER GYNECOLOGI

Page Type
Cleared 510(K)
510(k) Number
K854470
510(k) Type
Traditional
Applicant
MINNESOTA LASER CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/7/1986
Days to Decision
93 days

PORTALASE 300 CARBON DIOXIDE SURG LASER GYNECOLOGI

Page Type
Cleared 510(K)
510(k) Number
K854470
510(k) Type
Traditional
Applicant
MINNESOTA LASER CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/7/1986
Days to Decision
93 days