Last synced on 14 November 2025 at 11:06 pm

SHARPLAN 1030 SEALED CO2 SURGICAL LASER SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K896847
510(k) Type
Traditional
Applicant
SHARPLAN LASERS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/24/1990
Days to Decision
50 days

SHARPLAN 1030 SEALED CO2 SURGICAL LASER SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K896847
510(k) Type
Traditional
Applicant
SHARPLAN LASERS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/24/1990
Days to Decision
50 days