Last synced on 14 November 2025 at 11:06 pm

PORTALASE 200 CARBON DIOXIDE SURG LASER NEUROLOGIC

Page Type
Cleared 510(K)
510(k) Number
K854468
510(k) Type
Traditional
Applicant
MINNESOTA LASER CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/20/1986
Days to Decision
226 days

PORTALASE 200 CARBON DIOXIDE SURG LASER NEUROLOGIC

Page Type
Cleared 510(K)
510(k) Number
K854468
510(k) Type
Traditional
Applicant
MINNESOTA LASER CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/20/1986
Days to Decision
226 days