Last synced on 14 November 2025 at 11:06 pm

MODIFIED SHARPLAN MODEL 1020 CO2 LASER

Page Type
Cleared 510(K)
510(k) Number
K882180
510(k) Type
Traditional
Applicant
SHARPLAN LASERS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/2/1988
Days to Decision
30 days

MODIFIED SHARPLAN MODEL 1020 CO2 LASER

Page Type
Cleared 510(K)
510(k) Number
K882180
510(k) Type
Traditional
Applicant
SHARPLAN LASERS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/2/1988
Days to Decision
30 days